Generic sample preparation

ABSTRACT

The present invention relates to the sample preparation of nucleic acids for diagnostic purposes. More precisely, the invention provides a process for simultaneously isolating at least a first and a second target nucleic acid from a plurality of different types of fluid samples and optionally amplifying said isolated nucleic acids in a simultaneous manner.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent application Ser. No. 13/192,210, filed on Jul. 27, 2011, which claims the benefit of U.S. Provisional Application No. 61/368,970 filed on Jul. 29, 2010. The entire disclosures of the above-referenced prior application are hereby incorporated herein by reference in their entireties.

FIELD OF THE INVENTION

The present invention belongs to the field of in-vitro diagnostics. Within this field, it particularly concerns sample preparation of nucleic acids for diagnostic purposes. More precisely, the invention provides a process for simultaneously isolating at least a first and a second target nucleic acid from a plurality of different types of fluid samples.

BACKGROUND OF THE INVENTION

The isolation of biological materials such as nucleic acids or proteins from complex biological mixtures such as e.g. clinical samples has been of considerable significance especially for diagnostic purposes.

Examples for diagnostic applications of nucleic acid sample preparation comprise preparation and subsequent detection of viruses such as Human Papilloma Virus (HPV), West Nile Virus (WNV) or the routine screening of blood donations for the presence of Human Immunodeficiency Virus (HIV), Hepatitis-B (HBV) and/or C Virus (HCV). Furthermore, said amplification techniques are suitable for bacterial targets such as mycobacteria or Chlamydia trachomatis and Neisseria gonorrhoeae, or the analysis of oncology markers.

Numerous different methods have been developed in the art, e.g. denaturing, precipitating and removing undesired components in a sample with subsequent precipitation and isolation of the analyte in question (for example alcohol-based precipitation of nucleic acids). Another approach is the binding of the respective biological material to a solid support material which may be provided, e.g., in the form of chromatographic columns. For diagnostic purposes, and especially for the automated isolation of biological materials subject to subsequent medium- or high-throughput analysis, binding particles are often used. Such particles can have functionalized surfaces, i.e. they are often coated with antibodies, nucleic acid capture probes or the like, in order to bind the desired analyte. Alternatively, they may have unmodified surfaces such as glass surfaces particularly for the isolation of nucleic acids.

However, target nucleic acids to be analyzed for diagnostic purposes can be present in a variety of different sources. In practice, the sample preparation procedure for nucleic acids in different sources is usually adapted to

-   -   1. the type of fluid sample     -   2. the type of nucleic acid.

Other criteria may also have to be taken into account when isolating different nucleic acids from different sources. The prior art has addressed this diversity by providing different methods of preparation for said different types of samples.

An improved method for isolating at least a first and a second target nucleic acid from a plurality of different types of fluid samples is provided by the present invention.

SUMMARY OF THE INVENTION

The present invention provides a process for simultaneously isolating at least a first and a second target nucleic acid from a plurality of different types of samples, the process comprising the steps of:

-   -   a) combining a solid support material and the plurality of         different types of samples in a number of vessels corresponding         to number of samples for a period of time and under conditions         sufficient to permit nucleic acids comprising the target nucleic         acids to be immobilized on the solid support material,     -   b) isolating the solid support material from the other material         present in the samples in a separation station, and     -   c) purifying the nucleic acids in a separation station by         separating the sample from the solid support material and         washing the solid support material one or more times with a wash         buffer,         wherein the physical conditions and the period of time are         identical for the members of the plurality of different types of         samples.

In another embodiment, the process provides wherein step a) further comprises releasing nucleic acids from their cellular and/or viral environment by lysing cells and/or viral capsids that may be present in the plurality of different samples, wherein step a) further comprises the addition of a lysis buffer to the plurality of different samples, wherein the lysis buffer is identical for the members of the plurality of different types of samples, wherein the lysis buffer comprises one or more components selected from the group consisting of: a chaotropic agent, a buffer substance, an alcohol, and a reducing agent, and wherein the lysis buffer has an acidic pH.

In another embodiment, the invention provides a process wherein at least one sample of the plurality of different samples has a different volume than the other samples, and wherein the vessels are combined in the same integral arrangement. Further, in some embodiments the invention provides wherein the first target nucleic acid comprises RNA and the second target nucleic acid comprises DNA, wherein the first target nucleic acid and the second target nucleic acid are from different organisms.

Further, the invention provides wherein step a) is carried out at a temperature of up to 50° C., wherein the process further comprises after step c) the following step:

-   -   d) eluting the nucleic acids from the solid support material         with an elution buffer.

In another embodiment step d) is carried out at a temperature between 70° C. and 90° C. Further, the process further comprises after step c) or after step d) the following steps:

-   -   e) transferring the purified nucleic acids and optionally the         solid support material to a plurality of reaction vessels, and     -   f) amplifying the target nucleic acids.

In another embodiment, step f) comprises the following steps:

-   -   i) contacting the purified nucleic acids with one or more         amplification reagents comprising a polymerase with reverse         transcriptase activity, in at least two reaction vessels,         wherein at least a first reaction vessel comprises at least the         first target nucleic acid and at least a second reaction vessel         comprises at least the second target nucleic acid, and wherein         the second target nucleic acid is absent from the first reaction         vessel;     -   ii) incubating in the reaction vessels the purified nucleic         acids with the one or more amplification reagents for a period         of time, under conditions suitable for transcription of RNA by         the polymerase with reverse transcriptase activity to occur; and     -   iii) incubating in the reaction vessels the purified nucleic         acids with the one or more amplification reagents for a period         of time, under conditions sufficient for an amplification         reaction indicative of the presence or absence of the first and         second target nucleic acid to occur,         wherein the conditions for transcription and amplification in         steps i) to iii) are identical for the at least first and second         target nucleic acids. Further, in another embodiment the solid         support comprises nucleic acid binding particles.

DESCRIPTION OF THE INVENTION

The present invention provides a method for simultaneously isolating at least a first and a second target nucleic acid from a plurality of different types of fluid samples.

In a first aspect, the invention relates to a process for simultaneously isolating at least a first and a second target nucleic acid from a plurality of different types of fluid samples, said process comprising the automated steps of

-   -   b. combining together a solid support material and said         plurality of different types of fluid samples in a number of         vessels corresponding to the number of fluid samples for a         period of time and under conditions sufficient to permit nucleic         acids comprising the target nucleic acids to be immobilized on         the solid support material,     -   c. isolating the solid support material from the other material         present in the fluid samples in a separation station,     -   c. purifying the nucleic acids in a separation station by         separating the fluid sample from the solid support material and         washing the solid support material one or more times with a wash         buffer,         wherein the physical conditions and said period of time are         identical for the members of said plurality of different types         of fluid samples.

Especially, but not only for clinical laboratories with a high sample throughput, it is highly favorable to be provided with such an improved method for the quick, easy and reliable simultaneous isolation of multiple target nucleic acids from a plurality of different types of fluid samples.

The process comprising the automated steps mentioned above displays various advantages.

Firstly, the combination of the sample preparation procedure according to the present invention with e.g. reverse transcription of RNA and amplification of the target nucleic acids in an automated manner significantly reduces the need for manual intervention and thereby the potential risk of contamination.

Moreover, the possibility of providing a single process in which a variety of different samples, i.e. different sources of nucleic acids, contributes significantly to reduction of the overall complexity of nucleic acid diagnostic. If, for example, different methods have to be applied to every type of fluid sample, as it has been the case in the prior art, sample preparation is much more complex, time-consuming and resource-intensive. Mostly, different reagents have to be exploited, leading to increased costs and hampering the development of quick and uncomplicated automated solutions.

The sample preparation according to the invention exhibits the appropriate flexibility and workflow to deal with multiple different sample types containing different types of nucleic acids such as for example DNA and RNA.

Different sources, i.e. types of samples, comprise, among others, all kinds of human body fluids, such as for example blood, sputum, nasal swab, urine, sweat or others.

The process according to the invention requires considerably less hands-on time and testing is much simpler to perform than sample preparation methods used in the prior art. The process according to the invention offers a major advantage e.g. in the field of clinical virology as it permits parallel sample preparation and downstream amplification of several viruses in parallel experiments. The process is particularly useful in the management of post-transplant patients, in whom frequent viral monitoring is required. Thereby the process according to the invention facilitates cost-effective diagnosis and contributes to a decrease in the use of antiviral agents and in viral complications and hospitalizations. This equally applies to the field of clinical microbiology. In general, efficiencies will be gained in faster turnaround time and improved testing flexibility. Consequently, this leads to a decrease in the number of test runs requested on a patient to make a diagnosis, and potentially shorter hospital stays (e.g. if a diagnosis can be provided sooner, patients requiring antimicrobial therapy will receive it sooner and thus recover earlier). In addition, patients show less morbidity and therefore cause fewer costs related to supportive therapy (e.g., intensive care related to a delay in diagnosis of sepsis). Providing a negative result sooner can have important implications for the overprescription of antibiotics. For example, if a test result obtained using the process according to the invention is able rule out the pathogen more quickly than with a standard sample preparation method followed e.g. by real-time PCR, then the clinician will not be forced to use empirical antibiotics. Alternatively, if empirical antibiotics are used, the duration of the respective treatment can be shortened.

With respect to designing an assay including sample preparation with the process according to the invention, the skilled artisan will particularly, but not only, benefit from the following advantages:

-   -   a reduction in software complexity (leading to a reduced risk of         programming errors)     -   focusing of assay development efforts on the chemistry         optimization instead of the chemistry plus the instrument         control parameters     -   much more reliable system since a single process is always used         and the hardware can be optimally designed to perform this         protocol     -   the skilled artisan performing the process according to the         invention is provided with the flexibility to run multiple         different isolations in parallel as part of the same process     -   cost reduction.

In the sense of the invention, “purification”, “isolation” or “extraction” of nucleic acids relate to the following: Before nucleic acids may be analyzed in a diagnostic assay e.g. by amplification, they typically have to be purified, isolated or extracted from biological samples containing complex mixtures of different components. For the first steps, processes may be used which allow the enrichment of the nucleic acids.

Often, the nucleic acids to be analyzed are not free in solution within the fluid sample in question, but are located within closed structures such as for example cells or viruses. In diagnostic assays it is often the objective to identify especially pathogenic cells or viruses in fluid samples such as clinical samples. Such pathogens can e.g. comprise RNA viruses like for example Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV), the West Nile Virus (WNV), Human Papilloma Virus (HPV), Japanese Encephalitis Virus (JEV), St. Louis Encephalitis Virus (SLEV) and others, or DNA viruses like e.g. Hepatitis B Virus (HBC), Cytomegalovirus (CMV) and others, or bacteria like e.g. Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG) and others. The method according to the invention is useful for the extraction of nucleic acids from the above-mentioned as well as other organisms.

Therefore, an aspect of the invention is the process described supra, wherein step a. further comprises releasing nucleic acids from their cellular and/or viral environment by lysing cells and/or viral capsids potentially present in the plurality of different fluid samples.

To release the contents of cells or viral particles, they may be treated with enzymes or with chemicals to dissolve, degrade or denature the cellular walls or viral particles. This process is commonly referred to as lysis. The resulting solution containing such lysed material is referred to as lysate.

Agents suitable to lyse cells and/or viral capsids or similar structures are commonly provided within a lysis buffer. Hence, in an embodiment of the invention, the process described above further comprises in step a. the addition of a lysis buffer to the plurality of different fluid samples.

Since the method according to the invention is especially advantageous with respect to high throughput, efficiency and parallelization, an aspect of the invention is the process described above, wherein said lysis buffer is identical for the members of said plurality of different types of fluid samples.

That way, the complexity of the sample preparation procedure is further reduced, since no different lysis reagents have to be provided individually for the different samples to be treated. Furthermore, the procedure can be controlled more easily when working with a single lysis buffer. The lysis buffer can e.g. be withdrawn with a mulipipettor from a single container and subsequently be dispensed into the different samples simultaneously.

In an embodiment of the invention, the lysis buffer in the process described above comprises one or more components selected from the group of:

-   -   a chaotropic agent     -   a buffer substance     -   an alcohol     -   a reducing agent.

Chaotropic agents, which generally disturb the ordered structure of water molecules in solution and non-covalent binding forces in and between molecules, can make several contributions to the procedure of sample preparation. In particular, but not only, they can be applied as RNase inhibitors by disturbing the nuclease's tertiary structure. Usually, no further RNase inhibitor has to be applied to the lysis buffer. Besides, chaotropic agents contribute to the disruption of biological membranes, such as plasma membranes or the membranes of cell organelles if present. Also, they can play a significant role in the adhesive binding of nucleic acids to surfaces like glass (see infra). Exemplary chaotropic agents in the context of the invention are guanidinium salts like guanidinium thiocyanate or guanidinium hydrochloride or guanidinium chloride or guanidinium isothiocyanate, urea, perchlorates such as e.g. potassium perchlorate, other thiocyanates or potassium iodide. However, other chaotropic agents can also be used within the scope of the invention.

Buffer substances are generally important for maintaining a certain pH value or pH range in a solution. This is the prerequisite for most biological systems, and mostly also desirable for in vitro reactions. It can also be advantageous for the process of the invention. Exemplary buffers in the context of the invention are citrate buffers such as sodium citrate, but also Tris (Tris-(hydroxymethyl)-aminomethane) buffers such as Tris HCl, phosphate, N-(2-hydroxyethyl)-piperazine-N′-(2-ethanesulfonic acid) (HEPES), acetate buffers, but also other buffers can be used in the context of the invention.

The use of alcohol in a lysis buffer for nucleic acid preparation can also be advantageous, as known by the person skilled in the art. An example in the context of the invention is the use of polidocanol, while other alcohol may also be used in the lysis buffer described above. The use of polidocanol for the preparation of nucleic acids has e.g. been described in EP 1 932 913.

Reducing agents can also contribute to the denaturation of undesired components such as the RNase A mentioned above. In particular, reducing agents, as widely known in the art, cleave inter- and intramolecular disulfide bonds, which are especially important for the tertiary structure of many proteins. An example in the context of the invention are reducing agents such as dithiothreitol (DTT), but other reducing agents known in the art such as e.g. 2-mercaptoethanol can also be advantageously employed in the context of the invention.

In view of the aforementioned, an aspect of the invention is the process described above, wherein said lysis buffer comprises the following components:

-   -   Guanidinium thiocyanate,     -   NaCitrate,     -   polydocanol,     -   DTT.

In an embodiment of the invention, the concentrations of the above-mentioned components of the lysis buffer are as follows

-   -   Guanidinium thiocyanate: 4 M     -   NaCitrate: 50 mM     -   polydocanol: 5% w/v     -   DTT: 2% w/v.

The pH of the lysis buffer described above is not restricted to specific pH values. However, in a an embodiment, said lysis buffer has an acidic pH, or a pH between 5.5 and 6.5, or about 5.8.

A problem often encountered during lysis is that other enzymes degrading the component of interest, e.g. deoxyribonucleases or ribonucleases degrading nucleic acids such as the RNase mentioned supra, come into contact with the component of interest during the lysis procedure. These degrading enzymes may also be present outside the cells or may have been spatially separated in different cellular compartments prior to lysis. As the lysis takes place, the component of interest becomes exposed to said degrading enzymes. Other components released during this process may e.g. be endotoxins belonging to the family of lipopolysaccharides which are toxic to cells and can cause problems for products intended to be used in human or animal therapy.

There is a variety of means to tackle the above-mentioned problem. It is common to use chaotropic agents (as described supra) or anionic, cationic, zwitterionic or non-ionic detergents when nucleic acids are intended to be set free.

It is also an advantage to use proteases which rapidly degrade the previously described enzymes or unwanted proteins. However, this may produce another problem as said substances or enzymes can interfere with reagents or components in subsequent steps.

Enzymes which can be used in such lysis or sample preparation processes mentioned above are enzymes which cleave the amide linkages in protein substrates and which are classified as proteases, or (interchangeably) peptidases (see Walsh, 1979, Enzymatic Reaction Mechanisms. W. H. Freeman and Company, San Francisco, Chapter 3). Proteases used in the prior art comprise alkaline proteases (WO 98/04730) or acid proteases (U.S. Pat. No. 5,386,024). A protease which has been widely used for sample preparation in the isolation of nucleic acids in the prior art is proteinase K from Tritirachium album (see e.g. Sambrook J. et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989) which is active around neutral pH and belongs to a family of proteases known to the person skilled in the art as subtilisins. An example for the use in lysis or sample preparation processes mentioned above is the enzyme esperase, a robust protease that retains its activity at both high alkalinity and at high temperatures (EP 1 201 753).

In the sample preparation steps following the lysis step, the component of interest is further enriched. If the non-proteinaceous components of interest are e.g. nucleic acids, they are normally extracted from the complex lysis mixtures before they are used in a probe-based assay.

There are several methods for the purification of nucleic acids:

-   -   sequence-dependent or biospecific methods as e.g.:     -   affinity chromatography         -   hybridization to immobilized probes     -   sequence-independent or physico-chemical methods as e.g.:         -   liquid-liquid extraction with e.g. phenol-chloroform         -   precipitation with e.g. pure ethanol         -   extraction with filter paper         -   extraction with micelle-forming agents as             cetyl-trimethyl-ammonium-bromide         -   binding to immobilized, intercalating dyes, e.g. acridine             derivatives         -   adsorption to silica gel or diatomic earths         -   adsorption to magnetic glass particles (MGP) or             organo-silane particles under chaotropic conditions

Particularly interesting for purification purposes is the adsorption of nucleic acids to a glass surface although other surfaces are possible. Many procedures for isolating nucleic acids from their natural environment have been proposed in recent years by the use of their binding behavior to glass surfaces. If unmodified nucleic acids are the target, a direct binding of the nucleic acids to a material with a silica surface can be used because, among other reasons, the nucleic acids do not have to be modified, and even native nucleic acids can be bound. These processes are described in detail by various documents. In Vogelstein B. et al., Proc. Natl. Acad. USA 76 (1979) 615-9, for instance, a procedure for binding nucleic acids from agarose gels in the presence of sodium iodide to ground flint glass is proposed. The purification of plasmid DNA from bacteria on glass dust in the presence of sodium perchlorate is described in Marko M. A. et al., Anal. Biochem. 121 (1982) 382-387. In DE-A 37 34 442, the isolation of single-stranded M13 phage DNA on glass fiber filters by precipitating phage particles using acetic acid and lysis of the phage particles with perchlorate is described. The nucleic acids bound to the glass fiber filters are washed and then eluted with a methanol-containing Tris/EDTA buffer. A similar procedure for purifying DNA from lambda phages is described in Jakobi R. et al., Anal. Biochem. 175 (1988) 196-201. The procedure entails the selective binding of nucleic acids to glass surfaces in chaotropic salt solutions and separating the nucleic acids from contaminants such as agarose, proteins or cell residue. To separate the glass particles from the contaminants, the particles may be either centrifuged or fluids are drawn through glass fiber filters. This is a limiting step, however, that prevents the procedure from being used to process large quantities of samples. The use of magnetic particles to immobilize nucleic acids after precipitation by adding salt and ethanol is more advantageous and described e.g. in Alderton R. P. et al., S., Anal. Biochem. 201 (1992) 166-169 and PCT GB 91/00212. In this procedure, the nucleic acids are agglutinated along with the magnetic particles. The agglutinate is separated from the original solvent by applying a magnetic field and performing a wash step. After one wash step, the nucleic acids are dissolved in a Tris buffer. This procedure has a disadvantage, however, in that the precipitation is not selective for nucleic acids. Rather, a variety of solid and dissolved substances are agglutinated as well. As a result, this procedure can not be used to remove significant quantities of any inhibitors of specific enzymatic reactions that may be present. Magnetic, porous glass is also commercially available that contains magnetic particles in a porous, particular glass matrix and is covered with a layer containing streptavidin. This product can be used to isolate biological materials, e.g., proteins or nucleic acids, if they are modified in a complex preparation step so that they bind covalently to biotin. Magnetizable particular adsorbents proved to be very efficient and suitable for automatic sample preparation. Ferrimagnetic and ferromagnetic as well as superparamagnetic pigments are used for this purpose. An exemplary magnetic glass particles and methods using them are those described in WO 01/37291. Particularly useful for the nucleic acid isolation in the context of the invention is the method according to R. Boom et al. (J Clin Microbiol. 28 (1990), 495-503).

The flexibility of the process according to the invention can be further improved by adapting the volume of the respective fluid sample used in the process. This embodiment focuses on the diversity of the different types of fluid samples and possibly the types of organisms and nucleic acids present within them. E.g., certain viruses in a whole blood sample may require more starting material than other samples, if it is known that usually only low copy numbers are present in these specific cases.

Thus, an aspect of the invention is the process described above, wherein at least one fluid sample of said plurality of different fluid samples has a different volume than the other fluid samples.

In another embodiment, alternatively or additionally, different volumes of lysis buffer can be added to said plurality of different fluid samples.

In a further embodiment, when at least one fluid sample of said plurality of different fluid samples has a different volume than the other fluid samples, lysis buffer is added to the samples such that all samples have the same volume after addition.

In this embodiment, it is even more convenient to carry out an automated process on the different samples simultaneously. The advantages of being able to choose an appropriate starting volume depending on the sample type and of having identical volumes for carrying out the isolation and optionally e.g. amplification and detection are combined in this approach.

The term “solid support material” comprises any of the solid materials mentioned above in connection with the immobilization of nucleic acids, e.g. magnetic glass particles, glass fibers, glass fiber filters, filter paper etc., while the solid support material is not limited to these materials.

An aspect of the invention is the process described above, wherein the solid support material comprises nucleic acid binding particles, or one or more of the materials selected from silica, metal, metal oxides, plastic, polymers and nucleic acids. Or, the solid support material is magnetic glass particles.

“Immobilize”, in the context of the invention, means to capture objects such as e.g. nucleic acids in a reversible or irreversible manner. Particularly, “immobilized on the solid support material”, means that the object or objects are associated with the solid support material for the purpose of their separation from any surrounding media, and can be recovered e.g. by separation from the solid support material at a later point. In this context, “immobilization” can e.g. comprise the adsorption of nucleic acids to glass or other suitable surfaces of solid materials as described supra. Moreover, nucleic acids can be “immobilized” specifically by binding to capture probes, wherein nucleic acids are bound to essentially complementary nucleic acids attached to a solid support by base-pairing. In the latter case, such specific immobilization leads to the predominant binding of target nucleic acids.

“Simultaneously”, in the sense of the invention, means that two actions, such as amplifying a first and a second or more nucleic acids, are performed at the same time and under the same physical conditions. In one embodiment, simultaneous amplification of the at least first and second target nucleic acids is performed in one vessel. In another embodiment, simultaneous amplification is performed with at least one nucleic acid in one vessel and at least a second nucleic acid in a second vessel, at the same time and under the same physical conditions, particularly with respect to temperature and incubation time.

The “first target nucleic acid” and the “second target nucleic acid” are different nucleic acids.

A “fluid sample” is any fluid material that can be subjected to a diagnostic assay targeting nucleic acids and can be derived from a biological source. Also, said fluid sample can be derived from a human and is a body liquid. In an embodiment of the invention, the fluid sample is human blood, urine, sputum, sweat, swab, pipettable stool, or spinal fluid.

The term “reaction vessel” comprises, but is not limited to, tubes or the wells of plates such as microwell, deepwell or other types of multiwell plates, in which a reaction for the analysis of the fluid sample such as e.g. reverse transcription or a polymerase chain reaction takes place. The outer limits or walls of such vessels are chemically inert such that they do not interfere with the analytical reaction taking place within. In example, the isolation of the nucleic acids as described above is also carried out in a multiwell plate.

In this context, multiwell plates in analytical systems allow parallel separation and analyzing or storage of multiple samples. Multiwell plates may be optimized for maximal liquid uptake, or for maximal heat transfer. In example, a multiwell plate for use in the context of the present invention is optimized for incubating or separating an analyte in an automated analyzer. Further, the multiwell plate can be constructed and arranged to contact a magnetic device and/or a heating device.

Said multiwell plate, which is interchangeably termed “processing plate” in the context of the invention, comprises:

-   -   a top surface comprising multiple vessels with openings at the         top arranged in rows. The vessels comprise an upper part, a         center part and a bottom part. The upper part is joined to the         top surface of the multiwell plate and comprises two longer and         two shorter sides. The center part has a substantially         rectangular cross-section with two longer sides and two shorter         sides;     -   two opposing shorter and two opposing longer side walls and     -   a base, wherein said base comprises an opening constructed and         arranged to place the multiwell plate in contact with said         magnetic device and/or a heating device.

In an embodiment of the multiwell plate, adjacent vessels within one row are joined on the longer side of said almost rectangular shape.

In an embodiment, the multiwell plate comprises a continuous space which is located between adjacent rows of vessels. Said continuous space is constructed and arranged to accommodate a plate-shaped magnetic device. In an embodiment, the bottom part of the vessels comprises a spherical bottom. In an embodiment, the bottom part of said vessels comprises a conical part located between said central part and said spherical bottom.

In an embodiment, the top surface comprises ribs, wherein said ribs surround the openings of the vessels. In example, one shorter side of said upper part of the vessels comprises a recess, said recess comprising a bent surface extending from the rib to the inside of the vessel.

Furthermore, in an embodiment, the vessels comprise a rounded inside shape.

For fixation to the processing or incubation stations, the base may for example comprise a rim comprising recesses. Latch clips on a station of an analyzer can engage with said recesses to fix the plate on a station.

In an embodiment, the vessels comprise an essentially constant wall thickness.

The exemplary processing plate (101) in the context of the present invention is a 1-component plate. Its top surface (110) comprises multiple vessels (103) (FIG. 5, FIG. 6). Each vessel has an opening (108) at the top and is closed at the bottom end (112). The top surface (110) comprises ribs (104) which may beelevated relative to the top surface (110) and surround the openings (108) of the vessels (103). This prevents contamination of the contents of the vessels (103) with droplets of liquid that may fall onto the top surface (110) of the plate (101). Views of an exemplary process plate are shown in FIGS. 3 to 8.

The footprint of the processing plate (101) may comprise a length and width of the base corresponding to ANSI SBS footprint format. For example, the length is 127.76 mm+/−0.25 mm, and the width is 85.48 mm+/−0.25 mm. Thus, the plate (101) has two opposing shorter side walls (109) and two opposing longer side walls (118). The processing plate (101) comprises form locking elements (106) for interacting with a handler (500, FIG. 12). The processing plate (101) can be gripped, transported and positioned quickly and safely at high speed while maintaining the correct orientation and position. In example, the form locking elements (106) for gripping are located within the upper central part, the upper central third of the processing plate (101). This has the advantage that a potential distortion of the processing plate (101) has only a minor effect on the form locking elements (106) and that the handling of the plate (101) is more robust.

The processing plate (101) for example comprises hardware-identifiers (102) and (115). The hardware identifiers (102) and (115) are unique for the processing plate (101) and different from hardware identifiers of other consumables used in the same system. The hardware identifiers (102, 115) for example comprise ridges (119) and/or recesses (125) on the side walls of the consumables, wherein said pattern of ridges (119) and/or recesses (125) is unique for a specific type of consumable, for example the processing plate (101). This unique pattern is also referred to herein as a unique “surface geometry”. The hardware-identifiers (102, 115) ensure that the user can only load the processing plate (101) into the appropriate stacker position of an analytical instrument in the proper orientation. On the sides of processing plate (101), guiding elements (116) and (117) are comprised (FIG. 3, FIG. 4). They prevent canting of the processing plate (101). The guiding elements (116, 117) allow the user to load the processing plates (101) with guiding elements (116, 117) as a stack into an analytical instrument which is then transferred vertically within the instrument in a stacker without canting of the plates.

The center part (120) of the vessels (103) has an almost rectangular cross section (FIG. 6, FIG. 7). They are separated along the longer side (118) of the almost rectangular shape by a common wall (113) (FIG. 3). The row of vessels (103) formed thereby has the advantage that despite the limited space available, they have a large volume, for example 4 ml. Another advantage is that because of the essentially constant wall thickness, the production is very economical. A further advantage is that the vessels (103) strengthen each other and, thus, a high stability of the shape can be obtained.

Between the rows of vessels (103), a continuous space (121) is located (FIG. 6, FIG. 7). The space (121) can accommodate magnets (202, 203) or heating devices (128) (FIG. 11). These magnets (202, 203) and heating devices (128) are for example solid devices. Thus, magnetic particles (216) comprised in liquids (215) which can be held in the vessels (103) can be separated from the liquid (215) by exerting a magnetic field on the vessels (103) when the magnets (202, 203) are brought into proximity of the vessels (103). Or the contents of the vessels (103) can be incubated at an elevated, controlled temperature when the processing plate (101) is placed on the heating device (128). Since the magnets (202, 203) or heating devices (128) can be solid, a high energy density can be achieved. The almost rectangular shape of the central part (120) of the vessels (103) (FIG. 10) also optimizes the contact between the vessel wall (109) and a flat shaped magnet (202) or heating device (128) by optimizing the contact surface between vessel (103) and magnet (202) or heating device (128) and thus enhancing energy transfer into the vessel (103).

In the area of the conical bottom (111) of the vessels, the space (121) is even more pronounced and can accommodate further magnets (203). The combination of the large magnets (202) in the upper area and the smaller magnets (203) in the conical area of the vessels allows separation of magnetic particles (216) in larger or small volumes of liquid (215). The small magnets (203), thus, make it easier to sequester the magnetic particles (216) during eluate pipetting. This makes it possible to pipette the eluate with minimal loss by reducing the dead volume of the magnetic particle (216) pellet. Furthermore, the presence of magnetic particles (216) in the transferred eluate is minimized.

At the upper end of the vessels (103), one of the shorter side walls (109) of the vessel (103) comprises an reagent inlet channel (105) which extends to the circumferential rib (104) (FIGS. 3, 4, 7). The reagents are pipetted onto the reagent inlet channel (105) and drain off the channel (105) into the vessel (103). Thus, contact between the pipet needle or tip (3, 4) and liquid contained in the vessel is prevented. Furthermore, splashes resulting from liquid being directly dispensed into another liquid (215) contained in the vessels (103), which may cause contamination of the pipet needle or tip (3, 4) or neighboring vessels (103) is prevented. Sequential pipetting onto the reagent inlet channel (105) of small volumes of reagents followed by the largest volume of another reagent ensures that the reagents which are only added in small amounts are drained completely into the vessel (103). Thus, pipetting of small volumes of reagents is possible without loss of accuracy of the test to be performed.

On the inside, on the bottom of the vessels (111, 112), the shape becomes conical (111) and ends with a spherical bottom (112) (FIG. 6. FIG. 7). The inside shape of the vessel (114), including the rectangular center part (120), is rounded. The combination of spherical bottom (112), rounded inside shape (114), conical part (111) and refined surface of the vessels (103) leads to favorable fluidics which facilitate an effective separation and purification of analytes in the processing plate (101). The spherical bottom (112) allows an essentially complete use of the separated eluate and a reduction of dead-volume which reduces the carryover of reagents or sample cross-contamination.

The rim on the base (129) of the processing plate (101) comprises recesses (107) for engagement with latch clips (124) on the processing station (201) or heating device (128) or analytical instrument (126) (FIG. 5, FIG. 9). The engagement of the latch clips (124) with the recesses (107) allows positioning and fixation of the processing plate (101) on the processing station (201). The presence of the recesses (107) allows the latch force to act on the processing plate (101) almost vertically to the base (129). Thus, only small forces acting sideways can occur. This reduces the occurrence of strain, and, thus, the deformation of the processing plate (101). The vertical latch forces can also neutralize any deformations of the processing plate (101) leading to a more precise positioning of the spherical bottoms (111) within the processing station (201). In general, the precise interface between the processing plate (101) and the processing station (201) or heating device (128) within an analyzer reduces dead-volumes and also reduces the risk of sample cross-contamination.

A “separation station” is a device or a component of an analytical system allowing for the isolation of the solid support material from the other material present in the fluid sample. Such a separation station can e.g. comprise, but is not limited to, a centrifuge, a rack with filter tubes, a magnet, or other suitable components. In an embodiment of the invention, the separation station comprises one or more magnets. For example, one or more magnets are used for the separation of magnetic particles, for example magnetic glass particles, as a solid support. If, for example, the fluid sample and the solid support material are combined together in the wells of a multiwell plate, then one or more magnets comprised by the separation station can e.g. be contacted with the fluid sample itself by introducing the magnets into the wells, or said one or more magnets can be brought close to the outer walls of the wells in order to attract the magnetic particles and subsequently separate them from the surrounding liquid.

In an embodiment, the separation station is a device that comprises a multiwell plate comprising vessels with an opening at the top surface of the multiwell plate and a closed bottom. The vessels comprise an upper part, a center part and a bottom part, wherein the upper part is joined to the top surface of the multiwell plate and may comprise two longer and two shorter sides. The center part has a substantially rectangular cross-section with two longer sides, wherein said vessels are aligned in rows. A continuous space is located between two adjacent rows for selectively contacting at least one magnet mounted on a fixture with the side walls in at least two Z-positions. The device further comprises a magnetic separation station comprising at least one fixture. The fixture comprises at least one magnet generating a magnetic field. A moving mechanism is present which vertically moves said at least one fixture comprising at least one magnet at least between first and second positions with respect to the vessels of the multiwell plate. For example, said at least two Z-positions of the vessels comprise the side walls and the bottom part of said vessels. The magnetic field of said at least one magnet can draw the magnetic particles to an inner surface of the vessel adjacent to said at least one magnet when said at least one magnet is in said first position. The effect of said magnetic field is less when said at least one magnet is in said second position than when said at least one magnet is in said first position. For example, the fixture comprising said at least one magnet comprises a frame. The vessels may have features as described above in the context of multiwell plate/processing plate. One such feature is that at least a part of said vessels has a substantially rectangular cross-section orthogonal to the axis of said vessels.

In said first position, said at least one magnet is adjacent to said part of said vessels. Adjacent is understood to mean either in close proximity such as to exert a magnetic field on the contents of the vessel, or in physical contact with the vessel.

The separation station comprises a frame to receive the multiwell plate, and latch-clips to attach the multiwell plate. For example, the separation station comprises two types of magnets. This embodiment is further described below.

A second embodiment is described below, which comprises a spring which exerts a pressure on the frame comprising the magnets such that the magnets are pressed against the vessels of the multiwell plate.

The first magnets can be constructed and arranged to interact with vessels of a multiwell plate for exerting a magnetic field on a large volume of liquid comprising magnetic particles held in said vessels. Said second magnets can be constructed and arranged to interact with vessels of a multiwell plate for exerting a magnetic field on a small volume of liquid comprising magnetic particles held in said vessels. Said first and second magnets can be moved to different Z-positions.

Useful in the context of the present invention and said separation station is further a method of isolating and purifying a nucleic acid. The method comprises the steps of binding a nucleic acid to magnetic particles in a vessel of a multiwell plate. The vessel comprises an upper opening, a central part and a bottom part. The bound material is then separated from unbound material contained in a liquid when the major part of the liquid is located above the section where the conical part of the vessel is replaced by the central part with the rectangular shape, by moving a magnet from a second position to a first position and, in said first position, applying a magnetic field to the central part and, optionally, additionally applying a magnetic field to the bottom part of said vessel. The magnetic particles can optionally be washed with a washing solution. A small volume of liquid, wherein the major part of the liquid is located below the section where the conical part of the vessel is replaced by the central part with the rectangular shape is separated from said magnetic particles by selectively applying a magnetic field to the bottom part of said vessel.

Useful in the context of the present invention is also a magnetic separation station for separating a nucleic acid bound to magnetic particles, said separation station comprising first magnets which are constructed and arranged to interact with vessels of a multiwell plate for exerting a magnetic field on a large volume of liquid comprising magnetic particles held in said vessels, and second magnets constructed and arranged to interact with vessels of a multiwell plate for exerting a magnetic field on a small volume of liquid comprising magnetic particles held in said vessels, and wherein said first and second magnets can be moved to different Z-positions. Embodiments of the magnetic separation station are described herein.

An embodiment of a separation station (201) useful for the present invention is described below. The first embodiment of said separation station (201) comprises at least two types of magnets (202, 203). The first, long type of magnet (202) is constructed and arranged to fit into the space (121) of the processing plate (101). Magnet (202), thus, exerts a magnetic field on the liquid (215) in the vessel (103) to sequester magnetic particles (216) on the inside of the vessel wall. This allows separation of the magnetic particles (216) and any material bound thereto and the liquid (215) inside the vessel (103) when a large volume of liquid (215) is present. Magnet (202) has an elongated structure and is constructed and arranged to interact with the essentially rectangular central part (120) of the vessel. Thus, magnet (202) is used when the major part of the liquid (215) is located above the section where the conical part (111) of the vessel (103) is replaced by the central part (120) with the rectangular shape. As shown in FIG. 40, construction of the magnets (202) can comprise fixtures (204, 204 a) comprising magnets (202) which fit into the space (121) between the rows of vessels (103) in the processing plate (101). Another embodiment of magnets (202) comprises magnets (202) arranged on fixtures (204, 204 a). The magnets (203) of the separation station (201) are smaller, and can interact with the conical part (111) of the vessel (103). This is shown in FIG. 10. Magnets (203) can be arranged on a base (205) which can be moved into the space (121) of the processing plate (101). Each magnet (202, 203) can be constructed to interact with two vessels (103) in two adjacent rows. In an embodiment, the processing plate (101) has 6 rows of 8 vessels (103). A separation station (201) which can interact with the processing plate (101) has three fixtures (204, 204 a) comprising magnets (202) and four bases (205) comprising magnets (203). An embodiment is also included wherein the separation station has four magnetic fixtures (204, 204 a) comprising magnets (202) and three magnetic bases (205) comprising magnets (203).

The magnets (202, 203) are movable. The separation station (201) comprises a mechanism to move the fixtures (204, 204 a) and the bases (205). All fixtures (204, 204 a) are interconnected by a base (217) and are, thus, moved coordinately. All magnets (203) are joined to one base (218) and are, thus, moved coordinately. The mechanism for moving the magnetic plates (202) and (203) is constructed and arranged to move the two types of magnetic plates (202, 203) to a total of four end positions:

In FIG. 40 a-c, the magnets (203) are located in proximity of the conical part of the vessels (103) of the processing plate (101). This is the uppermost position of magnets (203), and is the separation position. In this Figure, the magnets (202) are located in the lowermost position. They are not involved in separation when they are in this position.

In the embodiment shown in FIG. 10, the base (217) of magnets (202) is connected to a positioning wheel (206). The base (217) comprises a bottom end (207) which is flexibly in contact with a connecting element (208) by a moving element (209). Said moving element is constructed and arranged to move the connecting element (208) along a rail (212) from one side to the other. Said moving element (209) is fixed to the connecting element (208) with a pin (220). Said connecting element (208) is fixed to the positioning wheel (206) by screw (210). Connecting element (208) is also connected to axis (211). Said connecting element (208) can be a rectangular plate. As the positioning wheel (206) moves eccentrically, around an axis (211), such that the screw (210) moves from a point above the eccentric axis to a point below the eccentric axis, moving element (209) and the bottom end (207) of the base (204) with the magnets (202) attached thereto are moved from the uppermost position to the lowermost position. The base (218) is mounted on a bottom part (219) and is connected, at its lower end, with pin (213) to a moving element (214), which can be a wheel, which interacts with the positioning wheel (206). When the positioning wheel (206) rotates around the axis (211), wheel (214) moves along positioning wheel (206). If the wheel (214) is located on a section of positioning wheel (206) where the distance from the axis (211) is short, the magnets (203) are in their lowermost position. When wheel (214) is located on a section of positioning wheel (206) where the distance from the axis (211) is at a maximum, the magnets (203) are in their uppermost position. Thus, in an embodiment of the first embodiment of the separation station, the location of the magnets (203) is controlled by the shape of the positioning wheel (206). When moving element (209) moves along the central, rounded upper or lower part (212 a) of rail (212), the small type of magnets (203) are moved up and down. When the moving element (209) is located on the side (212 b) of bottom end (207) and moves up or down, the magnets (202) are moved up- or downwards. The positioning wheel can be rotated by any motor (224).

In an embodiment, a spring (225) is attached to the base (222) of the separation station and the base (218) of magnets (203) to ensure that magnets (203) are moved into the lowermost position when they are moved downwards.

The term “pin” as used herein relates to any fixation element, including screws or pins.

In a second embodiment, the separation station (230) comprises at least one fixture (231) comprising at least one magnet (232), for example a number of magnets equal to a number of vessels (103) in a row (123). The separation station (230) can comprise a number of fixtures (231) equal to the number of rows (123) of the multiwell plate (101) hereinbefore described. For example, six fixtures (231) are mounted on the separation station (230). At least one magnet (232) is mounted on one fixture (231). For example, the number of magnets (232) equals the number of vessels (103) in one row (123). For example, eight magnets (232) are mounted on one fixture (231). For example, one type of magnet (232) is comprised on said fixture (231). For example, the magnet (232) is mounted on one side oriented towards the vessels with which the magnet interacts.

The fixture (231) is mounted on a base (233). Said mount may be flexible. The base (233) may comprise springs (234) mounted thereon. The number of springs (234) is at least one spring per fixture (231) mounted on said base (233). The base further comprises a chamfer (236) which limits the movement of the spring and, consequently, the fixture (231) comprising the magnets (232). For example, any one of said springs (234) is constructed and arranged to interact with a fixture (231).

For example, said spring (234) is a yoke spring. Said interaction controls the horizontal movement of the fixtures (231). Furthermore, the separation station (230) comprises a frame (235). The base (233) with fixtures (231) is connected to the frame (235) by a moving mechanism as described hereinbefore for the magnets (232) of the first embodiment.

For example, said base (233) and fixture (231) is constructed and arranged to move vertically (in Z-direction).

The multiwell plate (101) hereinbefore described is inserted into the separation station (230). The fixture (231) comprising the magnets (232) is moved vertically. Any one fixture (232) is, thus, moved into a space (121) between two rows (123) of vessels (103). The vertical movement brings the magnets (232) mounted on a fixture (231) into contact with the vessels (103). The Z-position is chosen depending on the volume of liquid (215) inside the vessels (103). For large volumes, the magnets (232) contact the vessels (103) in a center position (120) where the vessels (103) are of an almost rectangular shape. For small volumes of liquid (215) where the major part of the liquid (215) is located below the center part (120) of the vessels (103), the magnets (232) can contact the conical part (111) of the vessels (103).

A spring is attached to the base (233) of any one frame (231) (FIG. 9 a), b)). The spring presses the magnets (232) against the vessels (103). This ensures a contact between magnets (232) and vessels (103) during magnetic separation. For example, the magnet (232) contacts the vessel (103) on the side wall (109) located underneath the inlet (105). This has the advantage that liquid which is added by pipetting flows over the sequestered magnetic particles and ensures that particles are resuspended and that all samples in all vessels are treated identically.

This embodiment is particularly suited to separate a liquid (215) comprised in a multiwell plate (101) as hereinbefore described, from magnetic particles (216) when different levels of liquid (215) are contained in the vessels (103) of said multiwell plate (101).

A “wash buffer” is a fluid that is designed to remove undesired components, especially in a purification procedure. Such buffers are well known in the art. In the context of the purification of nucleic acids, the wash buffer is suited to wash the solid support material in order to separate the immobilized nucleic acid from any unwanted components. The wash buffer may, for example, contain ethanol and/or chaotropic agents in a buffered solution or solutions with an acidic pH without ethanol and/or chaotropic agents as described above. Often the washing solution or other solutions are provided as stock solutions which have to be diluted before use.

The washing in the process according to the invention requires a more or less intensive contact of the solid support material and the nucleic acids immobilized thereon with the wash buffer. Different methods are possible to achieve this, e.g. shaking the wash buffer with the solid support material in or along with the respective vessel or vessels. Another advantageous method is aspirating and dispensing the suspension comprising wash buffer and solid support material one or more times. This method is may be carried out using a pipet, wherein said pipet comprises a disposable pipet tip into which said suspension is aspirated and from which it is dispensed again. Such a pipet tip can be used several times before being discarded and replaced. Disposable pipet tips useful for the invention may have a volume of at least 10 μl, or at least 15 μl, or at least 100 μl, or at least 500 μl, or at least 1 ml, or about 1 ml. Pipets used in the context of the invention can also be pipetting needles.

Thus, an aspect of the invention is the process described above, wherein said washing in step c. comprises aspirating and dispensing the wash buffer comprising the solid support material.

For the ease of handling and to facilitate automation, the vessels mentioned above can be combined in an integral arrangement, so they can be manipulated together.

Consequently, an aspect of the invention is the process described above, wherein the vessels are combined in an integral arrangement.

Integral arrangements can e.g. be vials or tubes reversibly or irreversibly attached to each other or arranged in a rack. For example, the integral arrangement is a multiwell plate. For example, the multiwell plate is a deepwell plate.

The process according to the invention is particularly useful when different types of nucleic acids are to be prepared, since the provision of a single workflow and the same reagents abolishes the need to isolate different types of nucleic acids, like DNA and RNA, in an individual manner due to their different properties.

Thus, an aspect of the invention is the process mentioned above, wherein the first target nucleic acid comprises RNA and the second target nucleic acid comprises DNA.

Furthermore, multiple different fluid samples may comprise or be derived from different organisms. Also then it is advantageous to yield the respective nucleic acid simultaneously with the same workflow and reagents. The present invention allows for such simultaneous preparation of nucleic acids e.g. of bacteria, DNA viruses and RNA viruses despite their different structure and properties.

Hence, an aspect of the invention is the process described above, wherein the first target nucleic acid and the second target nucleic acid are from different organisms.

A further aspect of the invention is the process described above, wherein the first and/or the second nucleic acid is a non-viral nucleic acid.

Also, an aspect of the invention is the process described supra, wherein the first and/or the second target nucleic acid is a bacterial nucleic acid.

An “organism”, as used herein, means any living single- or multicellular life form. In the context of the invention, a virus is an organism.

The present invention is also useful when different nucleic acids are to be from the plurality of different types of fluid samples. Different nucleic acids can thus be isolated in parallel simultaneous extractions under the same physical conditions, and may then e.g. be further processed analytically in different vessels.

Thus, an aspect of the invention is the process described above, wherein the first nucleic acid is present in a first fluid sample, and the second nucleic acid is present in a second fluid sample.

Such an embodiment is particularly useful when said different nucleic acids are not in contact with each other and can be processed separately. Therefore, an aspect of the invention is the process described above, wherein the second target nucleic acid is absent from the first fluid sample.

However, different nucleic acids may also be present within the same sample, but not necessarily all of them have to be processed further after isolation. The present invention is also useful in these cases.

Hence, an aspect of the invention is the process described above, wherein the second nucleic acid is also present in the first fluid sample.

In the case of downstream processing, especially when using diagnostic techniques such as nucleic acid amplification methods, it is often desirable or even required to include one or more control nucleic acids. This way, either the analytical reaction can be controlled when adding the control to the purified nucleic acid, or also the sample preparation can be monitored when adding the control prior to or during the nucleic acid extraction. It is also common to include both types of controls.

In this respect, an aspect of the invention is the process described above, wherein a control nucleic acid is added to the fluid sample and/or the purified nucleic acid at any of the steps.

For binding the nucleic acids to the solid support material, and, if applicable, lysis of cells and viruses, it has proven advantageous to incubate at temperatures up to 50° C.

Thus, an aspect of the invention is the process described above, wherein step a. is carried out at a temperature of up to 50° C., or at a temperature between 35° C. and 45° C., or at a temperature of 40° C.

For downstream processing of the isolated nucleic acids, it can be advantageous to separate them from the solid support material before e.g. subjecting them to amplification.

Therefore, an aspect of the invention is the process described above, wherein said process further comprises after step c. the following step:

-   -   d. eluting the nucleic acids from the solid support material         with an elution buffer.

An “elution buffer” in the context of the invention is a suitable liquid for separating the nucleic acids from the solid support. Such a liquid may e.g. be distilled water or aqueous salt solutions, such as e.g. Tris buffers like Tris HCl, or HEPES, or other suitable buffers known to the skilled artisan. The pH value of such an elution buffer is alkaline or neutral. Said elution buffer may contain further components such as e.g. chelators like EDTA, which stabilizes the isolated nucleic acids by inactivation of degrading enzymes.

The elution is carried out at elevated temperatures, such that an embodiment of the invention is the process described above, wherein step d. is carried out at a temperature between 70° C. and 90° C., or at a temperature of 80° C.

As mentioned supra, it is often desirable to analyze the nucleic acids isolated by the process described above. For this, it can be advantageous to increase the amount of starting material for the analysis.

Therefore, an aspect of the invention is the process described above, wherein said process further comprises after step c. or after step d. the following steps:

-   -   e. transferring the purified nucleic acids and optionally said         solid support material to a plurality of reaction vessels     -   f. amplifying the target nucleic acids.

In this context, it is especially advantageous to employ amplification and detection methods which allow for simultaneous amplification and detection of multiple different nucleic acids in two or more reaction vessels under the same physical conditions and using the same reagents. A combination of such a technique with the fast and efficient sample preparation disclosed above can be very advantageous for providing e.g. integrated automated solutions, in which the same workflow is carried out on a plurality of different types of samples containing different nucleic acids. These samples can be processed in parallel to simultaneously isolate the different nucleic acids they contain, and the analysis of said isolated different nucleic acids may then also be carried out in a simultaneous manner. The combination of these approaches significantly reduces the complexity and time-to-result for such experiments, which is of considerable advantage particularly for diagnostic laboratories in a clinical setting.

Thus, an aspect of the invention is the process described above, wherein step f. comprises the following steps:

-   -   i. contacting the purified nucleic acids with one or more         amplification reagents comprising a polymerase with reverse         transcriptase activity in at least two reaction vessels, wherein         at least a first reaction vessel comprises at least said first         target nucleic acid and at least a second reaction vessel         comprises at least said second target nucleic acid and wherein         the second target nucleic acid is absent from the first reaction         vessel;     -   ii. incubating in said reaction vessels said purified nucleic         acids with said one or more amplification reagents for a period         of time and under conditions suitable for transcription of RNA         by said polymerase with reverse transcriptase activity to occur;     -   iii. incubating in said reaction vessels said purified nucleic         acids with said one or more amplification reagents for a period         of time and under conditions sufficient for an amplification         reaction indicative of the presence or absence of said first and         second target nucleic acid to occur,     -   wherein the conditions for transcription and amplification in         steps i. to iii. are identical for the at least first and second         target nucleic acids.

Regarding the amplification procedure, it has been a challenge in the prior art that the number of different target nucleic acids in a multiplex assay carried out in a single reaction vessel is limited by the number of appropriate labels. In a real-time PCR assay, for example, the potential overlap of fluorochrome spectra has a great impact on assay performance (risk of false positive results, lower precision etc.) Therefore, the respective fluorophores have to be carefully selected and spectrally well separated in order to assure the desired performance of a diagnostic test. Typically, the number of different usable fluorophores corresponds to a single-digit number of PCR instrument fluorescence channels.

In contrast, in the process described above, the amplification of at least a first and a second target nucleic acid takes place in at least two different reaction vessels, allowing for the simultaneous amplification of a higher number of different target nucleic acids, since signals in different reaction vessels can be detected independently from each other. Still, within the scope of the present invention are embodiments wherein in one or more of the multiple reaction vessels multiplex reactions are performed, thereby multiplying the number of targets that may be amplified simultaneously and under the same conditions.

“Amplification reagents”, in the context of the invention, are chemical or biochemical components that enable the amplification of nucleic acids. Such reagents comprise, but are not limited to, nucleic acid polymerases, buffers, mononucleotides such as nucleoside triphosphates, oligonucleotides e.g. as oligonucleotide primers, salts and their respective solutions, detection probes, dyes, and more.

As is known in the art, a “nucleoside” is a base-sugar combination. The base portion of the nucleoside is normally a heterocyclic base. The two most common classes of such heterocyclic bases are purines and pyrimidines.

“Nucleotides” are nucleosides that further include a phosphate group covalently linked to the sugar portion of the nucleoside. For those nucleosides that include a pentofuranosyl sugar, the phosphate group can be linked to either the 2′-, 3′- or 5′-hydroxyl moiety of the sugar. A nucleotide is the monomeric unit of an “oligonucleotide”, which can be more generally denoted as an “oligomeric compound”, or a “polynucleotide”, more generally denoted as a “polymeric compound”. Another general expression for the aforementioned is deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).

According to the invention, an “oligomeric compound” is a compound consisting of “monomeric units” which may be nucleotides alone or non-natural compounds (see below), more specifically modified nucleotides (or nucleotide analogs) or non-nucleotide compounds, alone or combinations thereof.

“Oligonucleotides” and “modified oligonucleotides” (or “oligonucleotide analogs”) are subgroups of oligomeric compounds. In the context of this invention, the term “oligonucleotide” refers to components formed from a plurality of nucleotides as their monomeric units. The phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide. The normal linkage or backbone of RNA and DNA is a 3′ to 5′ phosphodiester linkage. Oligonucleotides and modified oligonucleotides (see below) useful for the invention may be synthesized as principally described in the art and known to the expert in the field. Methods for preparing oligomeric compounds of specific sequences are known in the art, and include, for example, cloning and restriction of appropriate sequences and direct chemical synthesis. Chemical synthesis methods may include, for example, the phosphotriester method described by Narang S. A. et al., Methods in Enzymology 68 (1979) 90-98, the phosphodiester method disclosed by Brown E. L., et al., Methods in Enzymology 68 (1979) 109-151, the phosphoramidite method disclosed in Beaucage et al., Tetrahedron Letters 22 (1981) 1859, the H-phosphonate method disclosed in Garegg et al., Chem. Scr. 25 (1985) 280-282 and the solid support method disclosed in U.S. Pat. No. 4,458,066.

In the method according to the invention, the oligonucleotides may be chemically modified, i.e. the primer and/or the probe comprise a modified nucleotide or a non-nucleotide compound. The probe or the primer is then a modified oligonucleotide.

“Modified nucleotides” (or “nucleotide analogs”) differ from a natural nucleotide by some modification but still consist of a base, a pentofuranosyl sugar, a phosphate portion, base-like, pentofuranosyl sugar-like and phosphate-like portion or combinations thereof. For example, a label may be attached to the base portion of a nucleotide whereby a modified nucleotide is obtained. A natural base in a nucleotide may also be replaced by e.g. a 7-deazapurine whereby a modified nucleotide is obtained as well.

A “modified oligonucleotide” (or “oligonucleotide analog”), belonging to another specific subgroup of oligomeric compounds, possesses one or more nucleotides and one or more modified nucleotides as monomeric units. Thus, the term “modified oligonucleotide” (or “oligonucleotide analog”) refers to structures that function in a manner substantially similar to oligonucleotides and can be used interchangeably in the context of the present invention. From a synthetical point of view, a modified oligonucleotide (or an oligonucleotide analog) can for example be made by chemical modification of oligonucleotides by appropriate modification of the phosphate backbone, ribose unit or the nucleotide bases (Uhlmann and Peyman, Chemical Reviews 90 (1990) 543; Verma S., and Eckstein F., Annu. Rev. Biochem. 67 (1998) 99-134). Representative modifications include phosphorothioate, phosphorodithioate, methyl phosphonate, phosphotriester or phosphoramidate inter-nucleoside linkages in place of phosphodiester internucleoside linkages; deaza- or azapurines and -pyrimidines in place of natural purine and pyrimidine bases, pyrimidine bases having substituent groups at the 5 or 6 position; purine bases having altered substituent groups at the 2, 6 or 8 positions or 7 position as 7-deazapurines; bases carrying alkyl-, alkenyl-, alkinyl or aryl-moieties, e.g. lower alkyl groups such as methyl, ethyl, propyl, butyl, tert-butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, or aryl groups like phenyl, benzyl, naphtyl; sugars having substituent groups at, for example, their 2′ position; or carbocyclic or acyclic sugar analogs. Other modifications consistent with the spirit of this invention are known to those skilled in the art. Such modified oligonucleotides (or oligonucleotide analogs) are best described as being functionally interchangeable with, yet structurally different from, natural oligonucleotides. In more detail, exemplary modifications are disclosed in Verma S., and Eckstein F., Annu. Rev. Biochem. 67 (1998) 99-134 or WO 02/12263. In addition, modification can be made wherein nucleoside units are joined via groups that substitute for the internucleoside phosphate or sugar phosphate linkages. Such linkages include those disclosed in Verma S., and Eckstein F., Annu. Rev. Biochem. 67 (1998) 99-134. When other than phosphate linkages are utilized to link the nucleoside units, such structures have also been described as “oligonucleosides”.

A “nucleic acid” as well as the “target nucleic acid” is a polymeric compound of nucleotides as known to the expert skilled in the art. “Target nucleic acid” is used herein to denote a nucleic acid in a sample which should be analyzed, i.e. the presence, non-presence and/or amount thereof in a sample should be determined.

The term “primer” is used herein as known to the expert skilled in the art and refers to oligomeric compounds, primarily to oligonucleotides, but also to modified oligonucleotides that are able to prime DNA synthesis by a template-dependent DNA polymerase, i.e. the 3′-end of the e.g. primer provides a free 3′—OH group whereto further nucleotides may be attached by a template-dependent DNA polymerase establishing 3′- to 5′-phosphodiester linkage whereby deoxynucleoside triphosphates are used and whereby pyrophosphate is released.

A “probe” also denotes a natural or modified oligonucleotide. As known in the art, a probe serves the purpose to detect an analyte or amplificate. In the case of the process according to the invention, probes can be used to detect the amplificates of the target nucleic acids. For this purpose, probes typically carry labels.

“Labels”, often referred to as “reporter groups”, are generally groups that make a nucleic acid, in particular oligonucleotides or modified oligonucleotides, as well as any nucleic acids bound thereto distinguishable from the remainder of the sample (nucleic acids having attached a label can also be termed labeled nucleic acid binding compounds, labeled probes or just probes). Exemplary labels according to the invention are fluorescent labels, which are e.g. fluorescent dyes such as a fluorescein dye, a rhodamine dye, a cyanine dye, and a coumarin dye. Exemplary fluorescent dyes according to the invention are FAM, HEX, JA270, CAL635, Coumarin343, Quasar705, Cyan500, CY5.5, LC-Red 640, LC-Red 705.

In the context of the invention, any primer and/or probe may be chemically modified, i.e. the primer and/or the probe comprise a modified nucleotide or a non-nucleotide compound. The probe or the primer is then a modified oligonucleotide.

A method of nucleic acid amplification is the Polymerase Chain Reaction (PCR) which is disclosed, among other references, in U.S. Pat. Nos. 4,683,202, 4,683,195, 4,800,159, and 4,965,188. PCR typically employs two or more oligonucleotide primers that bind to a selected nucleic acid template (e.g. DNA or RNA). Primers useful for nucleic acid analysis include oligonucleotides capable of acting as a point of initiation of nucleic acid synthesis within the nucleic acid sequences of the target nucleic acids. A primer can be purified from a restriction digest by conventional methods, or it can be produced synthetically. The primer can be single-stranded for maximum efficiency in amplification, but the primer can be double-stranded. Double-stranded primers are first denatured, i.e., treated to separate the strands. One method of denaturing double stranded nucleic acids is by heating. A “thermostable polymerase” is a polymerase enzyme that is heat stable, i.e., it is an enzyme that catalyzes the formation of primer extension products complementary to a template and does not irreversibly denature when subjected to the elevated temperatures for the time necessary to effect denaturation of double-stranded template nucleic acids. Generally, the synthesis is initiated at the 3′ end of each primer and proceeds in the 5′ to 3′ direction along the template strand. Thermostable polymerases have e.g. been isolated from Thermus flavus, T. ruber, T. thermophilus, T. aquaticus, T. lacteus, T. rubens, Bacillus stearothermophilus, and Methanothermus fervidus. Nonetheless, polymerases that are not thermostable also can be employed in PCR assays provided the enzyme is replenished.

If the template nucleic acid is double-stranded, it is necessary to separate the two strands before it can be used as a template in PCR. Strand separation can be accomplished by any suitable denaturing method including physical, chemical or enzymatic means. One method of separating the nucleic acid strands involves heating the nucleic acid until it is predominately denatured (e.g., greater than 50%, 60%, 70%, 80%, 90% or 95% denatured). The heating conditions necessary for denaturing template nucleic acid will depend, e.g., on the buffer salt concentration and the length and nucleotide composition of the nucleic acids being denatured, but typically range from about 90° C. to about 105° C. for a time depending on features of the reaction such as temperature and the nucleic acid length. Denaturation is typically performed for about 5 sec to 9 min. In order to not expose the respective polymerase like e.g. the Z05 DNA Polymerase to such high temperatures for too long and thus risking a loss of functional enzyme, it can be preferred to use short denaturation steps.

In an embodiment of the invention, the denaturation step is up to 30 sec, or up to 20 sec, or up to 10 sec, or up to 5 sec, or about 5 sec.

If the double-stranded template nucleic acid is denatured by heat, the reaction mixture is allowed to cool to a temperature that promotes annealing of each primer to its target sequence on the target nucleic acids.

The temperature for annealing can be from about 35° C. to about 70° C., or about 45° C. to about 65° C.; or about 50° C. to about 60° C., or about 55° C. to about 58° C. Annealing times can be from about 10 sec to about 1 min (e.g., about 20 sec to about 50 sec; about 30 sec to about 40 sec). In this context, it can be advantageous to use different annealing temperatures in order to increase the inclusivity of the respective assay. In brief, this means that at relatively low annealing temperatures, primers may also bind to targets having single mismatches, so variants of certain sequences can also be amplified. This can be desirable if e.g. a certain organism has known or unknown genetic variants which should also be detected. On the other hand, relatively high annealing temperatures bear the advantage of providing higher specificity, since towards higher temperatures the probability of primer binding to not exactly matching target sequences continuously decreases. In order to benefit from both phenomena, in some embodiments of the invention the process described above comprises annealing at different temperatures, first at a lower, then at a higher temperature. If, e.g., a first incubation takes place at 55° C. for about 5 cycles, non-exactly matching target sequences may be (pre-)amplified. This can be followed e.g. by about 45 cycles at 58° C., providing for higher specificity throughout the major part of the experiment. This way, potentially important genetic variants are not missed, while the specificity remains relatively high.

The reaction mixture is then adjusted to a temperature at which the activity of the polymerase is promoted or optimized, i.e., a temperature sufficient for extension to occur from the annealed primer to generate products complementary to the nucleic acid to be analyzed. The temperature should be sufficient to synthesize an extension product from each primer that is annealed to a nucleic acid template, but should not be so high as to denature an extension product from its complementary template (e.g., the temperature for extension generally ranges from about 40° to 80° C. (e.g., about 50° C. to about 70° C.; about 60° C.). Extension times can be from about 10 sec to about 5 min, or about 15 sec to 2 min, or about 20 sec to about 1 min, or about 25 sec to about 35 sec. The newly synthesized strands form a double-stranded molecule that can be used in the succeeding steps of the reaction. The steps of strand separation, annealing, and elongation can be repeated as often as needed to produce the desired quantity of amplification products corresponding to the target nucleic acids. The limiting factors in the reaction are the amounts of primers, thermostable enzyme, and nucleoside triphosphates present in the reaction. The cycling steps (i.e., denaturation, annealing, and extension) may be repeated at least once. For use in detection, the number of cycling steps will depend, e.g., on the nature of the sample. If the sample is a complex mixture of nucleic acids, more cycling steps will be required to amplify the target sequence sufficient for detection. Generally, the cycling steps are repeated at least about 20 times, but may be repeated as many as 40, 60, or even 100 times.

Within the scope of the invention, a PCR can be carried out in which the steps of annealing and extension are performed in the same step (one-step PCR) or, as described above, in separate steps (two-step PCR). Performing annealing and extension together and thus under the same physical and chemical conditions, with a suitable enzyme such as, for example, the Z05 DNA polymerase, bears the advantage of saving the time for an additional step in each cycle, and also abolishing the need for an additional temperature adjustment between annealing and extension. Thus, the one-step PCR reduces the overall complexity of the respective assay.

In general, shorter times for the overall amplification can be preferred, as the time-to-result is reduced and leads to a possible earlier diagnosis.

Other nucleic acid amplification methods to be used in the context of the invention comprise the Ligase Chain Reaction (LCR; Wu D. Y. and Wallace R. B., Genomics 4 (1989) 560-69; and Barany F., Proc. Natl. Acad. Sci. USA 88 (1991) 189-193); Polymerase Ligase Chain Reaction (Barany F., PCR Methods and Applic. 1 (1991) 5-16); Gap-LCR (WO 90/01069); Repair Chain Reaction (EP 0439182 A2), 3SR (Kwoh D. Y. et al., Proc. Natl. Acad. Sci. USA 86 (1989) 1173-1177; Guatelli J. C., et al., Proc. Natl. Acad. Sci. USA 87 (1990) 1874-1878; WO 92/08808), and NASBA (U.S. Pat. No. 5,130,238). Further, there are strand displacement amplification (SDA), transcription mediated amplification (TMA), and Qb-amplification (for a review see e.g. Whelen A. C. and Persing D. H., Annu. Rev. Microbiol. 50(1996) 349-373; Abramson R. D. and Myers T. W., Curr Opin Biotechnol 4 (1993) 41-47).

A “polymerase with reverse transcriptase activity” is a nucleic acid polymerase capable of synthesizing DNA based on an RNA template. It is also capable of the formation of a double-stranded DNA once the RNA has been reverse transcribed into a single strand cDNA. In an embodiment of the invention, the polymerase with reverse transcriptase activity is thermostable.

In an embodiment, the process according to the invention comprises incubating a sample containing an RNA template with an oligonucleotide primer sufficiently complementary to said RNA template to hybridize with the latter, and a thermostable DNA polymerase in the presence of at least all four natural or modified deoxyribonucleoside triphosphates, in an appropriate buffer comprising a metal ion buffer which, in an embodiment, buffers both the pH and the metal ion concentration. This incubation is performed at a temperature sufficient for said primer to hybridize to said RNA template and said DNA polymerase to catalyze the polymerization of said deoxyribonucleoside triphosphates to form a cDNA sequence complementary to the sequence of said RNA template.

As used herein, the term “cDNA” refers to a complementary DNA molecule synthesized using a ribonucleic acid strand (RNA) as a template. The RNA may e.g. be mRNA, tRNA, rRNA, or another form of RNA, such as viral RNA. The cDNA may be single-stranded, double-stranded or may be hydrogen-bonded to a complementary RNA molecule as in an RNA/cDNA hybrid.

A primer suitable for annealing to an RNA template may also be suitable for amplification by PCR. For PCR, a second primer, complementary to the reverse transcribed cDNA strand, provides an initiation site for the synthesis of an extension product.

In the amplification of an RNA molecule by a DNA polymerase, the first extension reaction is reverse transcription using an RNA template, and a DNA strand is produced. The second extension reaction, using the DNA template, produces a double-stranded DNA molecule. Thus, synthesis of a complementary DNA strand from an RNA template by a DNA polymerase provides the starting material for amplification.

Thermostable DNA polymerases can be used in a coupled, one-enzyme reverse transcription/amplification reaction. The term “homogeneous”, in this context, refers to a two-step single addition reaction for reverse transcription and amplification of an RNA target. By homogeneous it is meant that following the reverse transcription (RT) step, there is no need to open the reaction vessel or otherwise adjust reaction components prior to the amplification step. In a non-homogeneous RT/PCR reaction, following reverse transcription and prior to amplification one or more of the reaction components such as the amplification reagents are e.g. adjusted, added, or diluted, for which the reaction vessel has to be opened, or at least its contents have to be manipulated. Both homogeneous and non-homogeneous embodiments are comprised by the scope of the invention.

Reverse transcription is an important step in an RT/PCR. It is, for example, known in the art that RNA templates show a tendency towards the formation of secondary structures that may hamper primer binding and/or elongation of the cDNA strand by the respective reverse transcriptase. Thus, relatively high temperatures for an RT reaction are advantageous with respect to efficiency of the transcription. On the other hand, raising the incubation temperature also implies higher specificity, i.e. the RT primers will not anneal to sequences that exhibit mismatches to the expected sequence or sequences. Particularly in the case of multiple different target RNAs, it can be desirable to also transcribe and subsequently amplify and detect sequences with single mismatches, e.g. in the case of the possible presence of unknown or rare substrains or subspecies of organisms in the fluid sample.

In order to benefit from both advantages described above, i.e. the reduction of secondary structures and the reverse transcription of templates with mismatches, it is one aspect of the invention to carry out the RT incubation at more than one different temperature.

Therefore, an aspect of the invention is the process described above, wherein in step ii. the incubation of the polymerase with reverse transcriptase activity is carried out at different temperatures from 30° C. to 75° C., or from 45° C. to 70° C., or from 55° C. to 65° C.

As a further important aspect of reverse transcription, long RT steps can damage the DNA templates that may be present in the fluid sample. If the fluid sample contains both RNA and DNA species, it is thus favorable to keep the duration of the RT steps as short as possible, but at the same time ensuring the synthesis of sufficient amounts of cDNA for the subsequent amplification and optional detection of amplificates.

Thus, an aspect of the invention is the process described above, wherein in step ii. the period of time is up to 30 minutes, 20 minutes, 15 minutes, 12.5 minutes, 10 minutes, 5 minutes, or 1 minute.

A further aspect of the invention is the process described above, wherein the polymerase with reverse transcriptase activity and comprising a mutation is selected from the group consisting of

-   -   a. a CS5 DNA polymerase     -   b. a CS6 DNA polymerase     -   c. a Thermotoga maritima DNA polymerase     -   d. a Thermus aquaticus DNA polymerase     -   e. a Thermus thermophilus DNA polymerase     -   f. a Thermus flavus DNA polymerase     -   g. a Thermus filiformis DNA polymerase     -   h. a Thermus sp. sps17 DNA polymerase     -   i. a Thermus sp. ZO5 DNA polymerase     -   j. a Thermotoga neapolitana DNA polymerase     -   k. a Termosipho africanus DNA polymerase     -   l. a Thermus caldophilus DNA polymerase

Particularly suitable for these requirements are enzymes carrying a mutation in the polymerase domain that enhances their reverse transcription efficiency in terms of a faster extension rate.

Therefore, an aspect of the invention is the process described above, wherein the polymerase with reverse transcriptase activity is a polymerase comprising a mutation conferring an improved nucleic acid extension rate and/or an improved reverse transcriptase activity relative to the respective wildtype polymerase.

In an embodiment, in the process described above, the polymerase with reverse transcriptase activity is a polymerase comprising a mutation conferring an improved reverse transcriptase activity relative to the respective wildtype polymerase.

Polymerases carrying point mutations that render them particularly useful in the context of the invention are disclosed in WO 2008/046612. In particular, polymerases to be used in the context of the present invention can be mutated DNA polymerases comprising at least the following motif in the polymerase domain:

T-G-R-L-S-S-X_(b7)-X_(b8)-P-N-L-Q-N; wherein X_(b8) is an amino acid selected from S or T and wherein X_(b8) is an amino acid selected from G, T, R, K, or L, wherein the polymerase comprises 3′-5′ exonuclease activity and has an improved nucleic acid extension rate and/or an improved reverse transcription efficiency relative to the wildtype DNA polymerase, wherein in said wildtype DNA polymerase X_(b8) is an amino acid selected from D, E or N.

One example is mutants of the thermostable DNA polymerase from Thermus species Z05 (described e.g. in U.S. Pat. No. 5,455,170), said variations comprising mutations in the polymerase domain as compared with the respective wildtype enzyme Z05. For example, a mutant Z05 DNA polymerase wherein the amino acid at position 580 is selected from the group consisting of G, T, R, K and L.

For reverse transcription using a thermostable polymerase, Mn2+ can be the divalent cation and is typically included as a salt, for example, manganese chloride (MnCl2), manganese acetate (Mn(OAc)2), or manganese sulfate (MnSO4). If MnCl2 is included in a reaction containing 50 mM Tricine buffer, for example, the MnCl2 is generally present at a concentration of 0.5-7.0 mM; 0.8-1.4 mM is preferred when 200 mM of each dGTP, dATP, dUTP, and, dCTP are utilized; and 2.5-3.5 mM MnCl2 is most preferred. Further, the use of Mg2+ as a divalent cation for reverse transcription is also preferred in the context of the present invention.

Since it is in the scope of the invention to reverse-transcribe RNA target nucleic acids into cDNA while preserving the DNA target nucleic acids so both cDNA and DNA can be used for subsequent amplification, the process according to the invention is particularly useful for the simultaneous amplification of target nucleic acids derived from both organisms having an RNA or organisms having a DNA genome. This advantage considerably increases the spectrum of different organisms, especially pathogens, that can be analyzed under identical physical conditions.

Therefore, an aspect of the invention is the process described above, wherein the at least two target nucleic acids comprise RNA and DNA.

Especially due to an appropriate temperature optimum, enzymes like Tth polymerase or, the mutant Z05 DNA polymerase mentioned above are suited to carry out the subsequent step of amplification of the target nucleic acids. Exploiting the same enzyme for both reverse transcription an amplification contributes to the ease of carrying out the process and facilitates its automation, since the fluid sample does not have to be manipulated between the RT and the amplification step.

Therefore, in an embodiment, in the process described above the same polymerase with reverse transcriptase activity is used in step ii. and step iii. For example, the enzyme is the mutant Z05 DNA polymerase described supra.

In order not to expose the polymerase or other components of the reaction mixture used in the context of the invention to elevated temperatures for times longer than necessary, in an embodiment, steps above 90° C. are up to 20 sec, or up to 15 sec, or up to 10 sec, or up to 5 sec or 5 sec long. This also reduces the time-to-result and cuts down the overall required time of the assay.

In such a homogeneous setup, it can be of considerable advantage to seal the reaction vessels prior to initiating the RT and the amplification, thereby reducing the risk of contamination. Sealing can be e.g. achieved by applying a foil that is transparent, a cap, or by oil added to the reaction vessels and forming a lipophilic phase as a sealing layer at the top of the fluid.

Thus, an aspect of the invention is the process described above, further comprising between step i. and step ii. the step of sealing the at least two reaction vessels.

The target of the amplification step can be an RNA/DNA hybrid molecule. The target can be a single-stranded or double-stranded nucleic acid. Although the most widely used PCR procedure uses a double-stranded target, this is not a necessity. After the first amplification cycle of a single-stranded DNA target, the reaction mixture contains a double-stranded DNA molecule consisting of the single-stranded target and a newly synthesized complementary strand. Similarly, following the first amplification cycle of an RNA/cDNA target, the reaction mixture contains a double-stranded cDNA molecule. At this point, successive cycles of amplification proceed as described above.

Since nucleic acid amplification, especially but not only in the case of PCR, is very efficient if carried out as a cycling reaction, an aspect of the invention is the process described above, wherein the amplification reaction in step iii. consists of multiple cycling steps.

Suitable nucleic acid detection methods are known to the expert in the field and are described in standard textbooks as Sambrook J. et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989 and Ausubel F. et al.: Current Protocols in Molecular Biology 1987, J. Wiley and Sons, NY. There may be also further purification steps before the nucleic acid detection step is carried out as e.g. a precipitation step. The detection methods may include but are not limited to the binding or intercalating of specific dyes as ethidium bromide which intercalates into the double-stranded DNA and changes its fluorescence thereafter. The purified nucleic acid may also be separated by electrophoretic methods optionally after a restriction digest and visualized thereafter. There are also probe-based assays which exploit the oligonucleotide hybridization to specific sequences and subsequent detection of the hybrid.

For example, the amplified target nucleic acids can be detected during or after the amplification reaction in order to evaluate the result of the analysis. Particularly for detection in real time, it is advantageous to use nucleic acid probes.

Thus, an aspect of the invention is the process described above, wherein a cycling step comprises an amplification step and a hybridization step, said hybridization step comprising hybridizing the amplified nucleic acids with probes.

It can be favorable to monitor the amplification reaction in real time, i.e. to detect the target nucleic acids and/or their amplificates during the amplification itself.

Therefore, an aspect of the invention is the process described above, wherein the probes are labeled with a donor fluorescent moiety and a corresponding acceptor fluorescent moiety.

The methods set out above can be based on Fluorescence Resonance Energy Transfer (FRET) between a donor fluorescent moiety and an acceptor fluorescent moiety. A representative donor fluorescent moiety is fluorescein, and representative corresponding acceptor fluorescent moieties include LC-Red 640, LC-Red 705, Cy5, and Cy5.5. Typically, detection includes exciting the sample at a wavelength absorbed by the donor fluorescent moiety and visualizing and/or measuring the wavelength emitted by the corresponding acceptor fluorescent moiety. In the process according to the invention, detection can be followed by quantitating the FRET. For example, detection is performed after each cycling step. For example, detection is performed in real time. By using commercially available real-time PCR instrumentation (e.g., LightCycler™ or TaqMan®), PCR amplification and detection of the amplification product can be combined in a single closed cuvette with dramatically reduced cycling time. Since detection occurs concurrently with amplification, the real-time PCR methods obviate the need for manipulation of the amplification product, and diminish the risk of cross-contamination between amplification products. Real-time PCR greatly reduces turn-around time and is an attractive alternative to conventional PCR techniques in the clinical laboratory.

The following patent applications describe real-time PCR as used in the LightCycler™ technology: WO 97/46707, WO 97/46714 and WO 97/46712. The LightCycler™ instrument is a rapid thermal cycler combined with a microvolume fluorometer utilizing high quality optics. This rapid thermocycling technique uses thin glass cuvettes as reaction vessels. Heating and cooling of the reaction chamber are controlled by alternating heated and ambient air. Due to the low mass of air and the high ratio of surface area to volume of the cuvettes, very rapid temperature exchange rates can be achieved within the thermal chamber.

TaqMan® technology utilizes a single-stranded hybridization probe labeled with two fluorescent moieties. When a first fluorescent moiety is excited with light of a suitable wavelength, the absorbed energy is transferred to a second fluorescent moiety according to the principles of FRET. The second fluorescent moiety is generally a quencher molecule. Typical fluorescent dyes used in this format are for example, among others, FAM, HEX, CY5, JA270, Cyan and CY5.5. During the annealing step of the PCR reaction, the labeled hybridization probe binds to the target nucleic acid (i.e., the amplification product) and is degraded by the 5′ to 3′ exonuclease activity of the Taq or another suitable polymerase as known by the skilled artisan, such as a mutant Z05 polymerase, during the subsequent elongation phase. As a result, the excited fluorescent moiety and the quencher moiety become spatially separated from one another. As a consequence, upon excitation of the first fluorescent moiety in the absence of the quencher, the fluorescence emission from the first fluorescent moiety can be detected.

In both detection formats described above, the intensity of the emitted signal can be correlated with the number of original target nucleic acid molecules.

As an alternative to FRET, an amplification product can be detected using a double-stranded DNA binding dye such as a fluorescent DNA binding dye (e.g., SYBRGREEN I® or SYBRGOLD® (Molecular Probes)). Upon interaction with the double-stranded nucleic acid, such fluorescent DNA binding dyes emit a fluorescence signal after excitation with light at a suitable wavelength. A double-stranded DNA binding dye such as a nucleic acid intercalating dye also can be used. When double-stranded DNA binding dyes are used, a melting curve analysis is usually performed for confirmation of the presence of the amplification product.

Molecular beacons in conjunction with FRET can also be used to detect the presence of an amplification product using the real-time PCR methods of the invention. Molecular beacon technology uses a hybridization probe labeled with a first fluorescent moiety and a second fluorescent moiety. The second fluorescent moiety is generally a quencher, and the fluorescent labels are typically located at each end of the probe. Molecular beacon technology uses a probe oligonucleotide having sequences that permit secondary structure formation (e.g. a hairpin). As a result of secondary structure formation within the probe, both fluorescent moieties are in spatial proximity when the probe is in solution. After hybridization to the amplification products, the secondary structure of the probe is disrupted and the fluorescent moieties become separated from one another such that after excitation with light of a suitable wavelength, the emission of the first fluorescent moiety can be detected.

Thus, in a method according to the invention is the method described above using FRET, wherein said probes comprise a nucleic acid sequence that permits secondary structure formation, wherein said secondary structure formation results in spatial proximity between said first and second fluorescent moiety.

Efficient FRET can only take place when the fluorescent moieties are in direct local proximity and when the emission spectrum of the donor fluorescent moiety overlaps with the absorption spectrum of the acceptor fluorescent moiety.

Thus, in an embodiment of the invention, said donor and acceptor fluorescent moieties are within no more than 5 nucleotides of each other on said probe.

In a further embodiment, said acceptor fluorescent moiety is a quencher.

As described above, in the TaqMan format, during the annealing step of the PCR reaction, the labeled hybridization probe binds to the target nucleic acid (i.e., the amplification product) and is degraded by the 5′- to 3′-exonuclease activity of the Taq or another suitable polymerase as known by the skilled artisan, such as a mutant Z05 polymerase, during the subsequent elongation phase.

Thus, in an embodiment, in the method according to the invention, amplification employs a polymerase enzyme having 5′- to 3′-exonuclease activity.

It is further advantageous to carefully select the length of the amplicon that is yielded as a result of the process described above. Generally, relatively short amplicons increase the efficiency of the amplification reaction. Thus, an aspect of the invention is the process described above, wherein the amplified fragments comprise up to 450 bases, up to 300 bases, up to 200 bases, and or up to 150 bases.

According to the invention it can further be of advantage to use control nucleic acids. It is known in the art that both qualitative and quantitative controls are of considerable significance particularly in a diagnostic environment.

In this context, a control nucleic acid serving as a “quantitative standard nucleic acid” is apt to be and used as a reference in order to quantify, i.e. to determine the quantity of the target nucleic acids. For this purpose, one or more quantitative standard nucleic acids undergo all possible sample preparation steps along with the target nucleic acids. Moreover, a quantitative standard nucleic acid is processed throughout the method within the same reaction mixture. It must generate, directly or indirectly, a detectable signal both in the presence or absence of the target nucleic acid. For this purpose, the concentration of the quantitative standard nucleic acid has to be carefully optimized in each test in order not to interfere with sensitivity but in order to generate a detectable signal also e.g. at very high target concentrations. In terms of the limit of detection (LOD, see below) of the respective assay, the concentration range for the “quantitative standard nucleic acid” is 20-5000×LOD, or 20-1000×LOD, or 20-5000×LOD. The final concentration of the quantitative standard nucleic acid in the reaction mixture is dependent on the quantitative measuring range accomplished. The quantitative standard nucleic acid can be, for example, DNA, RNA or PNA, armored DNA or RNA and modified forms thereof.

“Limit of detection” or “LOD” means the lowest detectable amount or concentration of a nucleic acid in a sample. A low “LOD” corresponds to high sensitivity and vice versa. The “LOD” is usually expressed either by means of the unit “cp/ml”, particularly if the nucleic acid is a viral nucleic acid, or as IU/ml. “Cp/ml” means “copies per milliliter” wherein a “copy” is copy of the respective nucleic acid. IU/ml stands for “International units/ml”, referring to the WHO standard.

A widely used method for calculating an LOD is “Probit Analysis”, which is a method of analyzing the relationship between a stimulus (dose) and the quantal (all or nothing) response. In a typical quantal response experiment, groups of animals are given different doses of a drug. The percent dying at each dose level is recorded. These data may then be analyzed using Probit Analysis. The Probit Model assumes that the percent response is related to the log dose as the cumulative normal distribution. That is, the log doses may be used as variables to read the percent dying from the cumulative normal. Using the normal distribution, rather than other probability distributions, influences the predicted response rate at the high and low ends of possible doses, but has little influence near the middle.

The Probit Analysis can be applied at distinct “hitrates”. As known in the art, a “hitrate” is commonly expressed in percent [%] and indicates the percentage of positive results at a specific concentration of an analyte. Thus for example, an LOD can be determined at 95% hitrate, which means that the LOD is calculated for a setting in which 95% of the valid results are positive.

In an embodiment, the method described above provides an LOD of 1 to 100 cp/ml or 0.5 to 50 IU/ml, of 1 to 75 cp/ml or 0.5 to 30 IU/ml, of 1 to 25 cp/ml or 1 to 20 IU/ml.

With respect to some examples of possible target nucleic acids from certain viruses, the method according to the invention may provide the following LODs:

-   -   HIV: up to 60 cp/ml, up to 50 cp/ml, up to 40 cp/ml, up to 30         cp/ml, up to 20 cp/ml, or up to 15 cp/ml     -   HBV: up to 10 IU/ml, up to 7.5 IU/ml, or up to 5 IU/ml     -   HCV: up to 10 IU/ml, up to 7.5 IU/ml, or up to 5 IU/ml     -   WNV I: up to 20 cp/ml, up to 15 cp/ml, or up to 10 cp/ml     -   WNV II: up to 20 cp/ml, up to 15 cp/ml, up to 10 cp/ml, or up to         5 cp/ml     -   JEV: up to 100 cp/ml, up to 75 cp/ml, up to 50 cp/ml, or up to         30 cp/ml     -   SLEV: up to 100 cp/ml, up to 75 cp/ml, up to 50 cp/ml, up to 25         cp/ml, or up to 10 cp/ml.

An example of how to perform calculation of quantitative results in the TaqMan format based on a quantitative standard nucleic acid is described in the following: A titer is calculated from input data of instrument-corrected fluorescence values from an entire PCR run. A set of samples containing a target nucleic acid and a control nucleic acid serving as a quantitative standard nucleic acid undergo PCR on a thermocycler using a specified temperature profile. At selected temperatures and times during the PCR profile samples are illuminated by filtered light and the filtered fluorescence data are collected for each sample for the target nucleic acid and the quantitative standard nucleic acid. After a PCR run is complete, the fluorescence readings are processed to yield one set of dye concentration data for the quantitative standard nucleic acid and one set of dye concentration data for the target nucleic acid. Each set of dye concentration data is processed in the same manner. After several plausibility checks, the elbow values (CT) are calculated for the quantitative standard nucleic acid and the target nucleic acid. The elbow value is defined as the point where the fluorescence of the target nucleic acid or the quantitative standard nucleic acid crosses a predefined threshold (fluorescence concentration). Titer determination is based on the assumptions that the target nucleic acid and the quantitative standard nucleic acid are amplified with the same efficiency and that at the calculated elbow value equal amounts of amplicon copies of target nucleic acid and quantitative standard nucleic acid are amplified and detected. Therefore, the (CTQS−CTtarget) is linear to log (target conc/QS conc), wherein “QS” stands for the internal quantitative standard nucleic acid. The titer T can then be calculated for instance by using a polynomial calibration formula as in the following equation:

T′=10(a(CTQS−CTtarget)2+b(CTQS−CTtarget)+c)

The polynomial constants and the concentration of the quantitative standard nucleic acid are known, therefore the only variable in the equation is the difference (CTQS−CTtarget).

In addition to mere detection of the presence or absence of a target nucleic acid in a fluid sample, it is often important to determine the quantity of said nucleic acid. As an example, stage and severity of a viral disease may be assessed on the basis of the viral load. Further, monitoring of any therapy requires information on the quantity of a pathogen present in an individual in order to evaluate the therapy's success.

In view of the above-mentioned, an aspect of the invention is the process described above, further comprising the step of determining the quantity of the target nucleic acids after step iii.

Further, in the sense of the invention, one or more control nucleic acids can serve as a “qualitative internal control nucleic acid”. Qualitative detection of a nucleic acid in a biological sample is crucial e.g. for recognizing an infection of an individual. Thereby, one important requirement for an assay for detection of a microbial infection is that false-negative or false-positive results be avoided, since such results would almost inevitably lead to severe consequences with regard to treatment of the respective patient. Thus, especially in PCR-based methods, a qualitative internal control nucleic acid is added to the detection mix. Said control is particularly important for confirming the validity of a test result: At least in the case of a negative result with regard to the respective target nucleic acid, the qualitative internal control reaction has to perform reactive within given settings, i.e. the qualitative internal control must be detected, otherwise the test itself is considered to be inoperative.

However, in a qualitative setup, said qualitative internal control does not necessarily have to be detected in case of a positive result. For qualitative tests, it is especially important that the sensitivity of the reaction is guaranteed and therefore strictly controlled As a consequence, the concentration of the qualitative internal control must be relatively low so that even in a situation e.g. of slight inhibition the qualitative internal control is not be detected and therefore the test is invalidated. It has to be carefully adapted to the respective assay and its sensitivity. For example, the concentration range for the qualitative internal nucleic acid, i.e. the second control nucleic acid, will comprise a range of 1 copy per reaction to 1000 copies per reaction. In relation to the respective assay's limit of detection (LOD), its concentration can be between the LOD of an assay and the 25 fold value of the LOD, or between the LOD and 10×LOD. Or, it is between 2× and 10×LOD. Or, it is between 5× and 10×LOD. Or, it is 5× or 10×LOD.

Thus, an aspect of the invention is the process described above, wherein the presence of an amplification product of said internal control nucleic acid is indicative of an amplification occurring in the reaction mixture even in the absence of amplification products for one or more of said target nucleic acids.

The present invention is especially useful for the development of simultaneous assays on a plurality of parameters and/or nucleic acid types while using the same internal control nucleic acid sequence for said different parameters and/or nucleic acid types. Therefore, it contributes to reducing the overall complexity of the corresponding experiments on various levels: For instance, only one internal control nucleic acid sequence has to be designed and added to the respective amplification mixes, thus saving the time and costs for designing and synthesizing or buying multiple control nucleic acid sequences. The assay or assays can be streamlined, and the risk of handling errors is reduced. In addition, the more different control nucleic acid sequences are employed in one assay or parallel assays carried out simultaneously under the same conditions, the more complex it may result to adjust the respective conditions. Moreover, with a single control suitable for a plurality of nucleic acids, said control can be dispensed from a single source e.g. into different vessels containing said different target nucleic acids. Within the scope of the invention, the single control nucleic acid sequence may also serve as a qualitative and as a quantitative control.

Thus, an aspect of the invention is a process for isolating and simultaneously amplifying at least a first and a second target nucleic acid that may be present in one or more fluid samples, said process comprising the automated steps of:

-   -   a. adding an internal control nucleic acid to each of said fluid         samples     -   b. combining together a solid support material and said one or         more fluid samples in one or more vessels for a period of time         and under conditions sufficient to permit nucleic acids         comprising the target nucleic acids and the internal control         nucleic acid to be immobilized on the solid support material     -   c. isolating the solid support material from the other material         present in the fluid samples in a separation station     -   d. purifying the nucleic acids in said separation station and         washing the solid support material one or more times with a wash         buffer     -   e. contacting the purified target nucleic acids and the purified         internal control nucleic acid with one or more amplification         reagents comprising at least one distinct set of primers for         each of said target nucleic acids and for said internal control         nucleic acid in at least two reaction vessels, wherein at least         a first reaction vessel comprises at least said first target         nucleic acid and at least a second reaction vessel comprises at         least said second target nucleic acid and wherein the second         target nucleic acid is absent from the first reaction vessel     -   f. incubating in said reaction vessel said purified target         nucleic acids and said purified internal control nucleic acid         with said one or more amplification reagents for a period of         time and under conditions sufficient for an amplification         reaction indicative of the presence or absence of said target         nucleic acids to occur,     -   g. detecting and measuring signals generated by the         amplification products of said target nucleic acids and being         proportional to the concentration of said target nucleic acids,         and detecting and measuring a signal generated by said internal         control nucleic acid,         wherein the conditions for amplification and detection in         steps d. to g. are identical for said at least first and second         purified target nucleic acids and said internal control nucleic         acid, and wherein the sequence of said internal control nucleic         acid is identical for said at least first and second purified         target nucleic acids.

As a further advantage of the method described above, the testing of a particular biological sample for other nucleic acids in possible subsequent experiments need not involve another sample preparation procedure with the addition of a different internal control nucleic acid, since the control used in the invention can be used to control the amplification of different nucleic acids. Thus, once an internal control nucleic acid has been added, other parameters may be tested in the same sample under the same conditions.

The internal control nucleic acid can be competitive, non-competitive or partially competitive.

A competitive internal control nucleic acid carries essentially the same primer binding sites as the target and thus competes for the same primers with the target. While this principle allows a good mimicry of the respective target nucleic acid due to their similar structure, it can lower the amplification efficiency with regard to the target nucleic acid or acids and thus lead to a less sensitive assay.

A non-competitive internal control nucleic acid has different primer binding sites than the target and thus binds to different primers. Advantages of such a setup comprise, among others, the fact that the single amplification events of the different nucleic acids in the reaction mixture can take place independently from each other without any competition effects. Thus, no adverse effects occur regarding the limit of detection of the assay as can be the case in a competitive setup.

Finally, in an amplification using a partially competitive setup the respective control nucleic acid and at least one of the target nucleic acids compete for the same primers, while at least one other target nucleic acid binds to different primers.

The fact that the method described above involves a distinct set of primers for each of said target nucleic acids and for said internal control nucleic acid renders the method considerably flexible. In this non-competitive setup it is not necessary to introduce target-specific binding sites into the control nucleic acid as in the case of a competitive setup, and the drawbacks of a competitive setup as mentioned above are avoided. In a non-competitive setup, the internal control nucleic acid has a sequence different from any target sequences, in order not to compete for their primers and/or probes. For example, the sequence of the internal control nucleic acid is different from the other nucleic acid sequences in the fluid sample. As an example, if the fluid sample is derived from a human, the internal control nucleic acid may not have a sequence which also endogenously occurs within humans. The difference in sequence should thus be at least significant enough to not allow the binding of primers and/or probes to the respective endogenous nucleic acid or acids under stringent conditions and thus render the setup competitive. In order to avoid such interference, the sequence of the internal control nucleic acid used in the invention can be derived from a source different from the origin of the fluid sample. For example, it is derived from a naturally occurring genome, for example a plant genome, or from a grape genome. In an embodiment, a nucleic acid derived from a naturally occurring genome is scrambled. As known in the art, “scrambling” means introducing base mutations in a sequence to a certain extent. For example, the sequence of the internal control nucleic acid used in the invention is substantially altered with respect to the naturally occurring gene it is derived from.

In the context of the invention, a “sequence” is the primary structure of a nucleic acid, i.e. the specific arrangement of the single nucleobases of which the respective nucleic acids consists. It has to be understood that the term “sequence” does not denote a specific type of nucleic acid such as

RNA or DNA, but applies to both as well as to other types of nucleic acids such as e.g. PNA or others. Where nucleobases correspond to each other, particularly in the case of uracil (present in RNA) and thymine (present in DNA), these bases can be considered equivalent between RNA and DNA sequences, as well-known in the pertinent art.

Clinically relevant nucleic acids are often DNA which can be derived e.g. from DNA viruses like e.g. Hepatitis B Virus (HBV), Cytomegalovirus (CMV) and others, or bacteria like e.g. Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG) and others. In such cases, it can be advantageous to use an internal control nucleic acid consisting of DNA, in order to reflect the target nucleic acids properties.

Therefore, an aspect of the invention is the method described above, wherein said internal control nucleic acid is DNA.

On the other hand, numerous nucleic acids relevant for clinical diagnostics are ribonucleic acids, like e.g. the nucleic acids from RNA viruses such as for example Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV), the West Nile Virus (WNV), Human Papilloma Virus (HPV), Japanese Encephalitis Virus (JEV), St. Louis Encephalitis Virus (SLEV) and others. The present invention can be readily applied to such nucleic acids. In this case, it can be advantageous to use an internal control nucleic acid consisting of RNA, in order to reflect the target nucleic acids properties. If both RNA and DNA are to be analyzed in the process described supra, the internal control nucleic acid can be RNA, as the internal control nucleic acid mimics the most sensitive target of an assay involving multiple targets, and RNA targets usually have to be more closely controlled.

Thus, an aspect of the invention is the method described above, wherein said internal control nucleic acid is RNA.

Since RNA is more prone to degradation than DNA due to influences such as alkaline pH, ribonucleases etc., internal control nucleic acids made of RNA can be provided as armored particles. Armored particles such as especially armored RNA are described e.g. in EP910643. In brief, the RNA, which can be produced chemically or heterologously e.g. by bacteria such as e.g. E. coli, is at least partially encapsulated in a viral coat protein. The latter confers resistance of the RNA towards external influences, in particular ribonucleases. It must be understood that internal control DNA can also be provided as an armored particle. Both armored RNA and DNA are useful as internal control nucleic acids in the context of the invention. In an embodiment, RNA control nucleic acids are armored with the MS2 coat protein in E. coli. In a further embodiment, DNA control nucleic acids are armored using lambda phage GT11.

Therefore, an aspect of the invention is the method described above, wherein said internal control nucleic acid is an armored nucleic acid.

The results of the assays described above may be adulterated and, for example, comprise false-positives, in the case of cross-contamination with nucleic acids from sources other than the fluid sample. In particular, amplificates of former experiments may contribute to such undesired effects. One particular method for minimizing the effects of cross-contamination of nucleic acid amplification is described in U.S. Pat. No. 5,035,996. The method involves the introduction of unconventional nucleotide bases, such as dUTP, into the amplified product and exposing carryover products to enzymatic and/or physicochemical treatment to render the product DNA incapable of serving as a template for subsequent amplifications. Enzymes for such treatments are known in the art. For example, uracil-DNA glycosylase, also known as uracil-N-glycosylase or UNG, removes uracil residues from PCR products containing that base. The enzyme treatment results in degradation of the contaminating carryover PCR product and serves to “sterilize” the amplification reaction.

Thus, an aspect of the invention is the process described above, further comprising between step i. and step ii. the steps of

-   -   treating the fluid sample with an enzyme under conditions in         which products from amplifications of cross-contaminating         nucleic acids from other samples are enzymatically degraded;     -   inactivating said enzyme.

For example, the enzyme is uracil-N-glycosylase.

For example, in the processes described above, all steps can be automated. “Automated” means that the steps of a process are suitable to be carried out with an apparatus or machine capable of operating with little or no external control or influence by a human being. Only the preparation steps for the method may have to be done by hand, e.g. storage containers have to be filled and put into place, the choice of samples has to be performed by a human being and further steps known to the expert in the field, e.g. the operation of a controlling computer. The apparatus or machine may e.g. automatically add liquids, mix the samples or carry out incubation steps at specific temperatures. Typically, such a machine or apparatus is a robot controlled by a computer which carries out a program in which the single steps and commands are specified.

A further aspect of the invention is an analytical system (440) for isolating and simultaneously amplifying at least two target nucleic acids that may be present in a fluid sample, said analytical system comprising the following modules:

-   -   a separation station (230) comprising a solid support material,         said separation station being constructed and arranged to         separate and purify a target nucleic acid comprised in a fluid         sample     -   an amplification station (405) comprising at least two reaction         vessels, said reaction vessels comprising amplification         reagents, at least a first purified target nucleic acid in at         least a first reaction vessel and at least a second purified         nucleic acid in at least a second reaction vessel, wherein the         second nucleic acid is absent from the first reaction vessel,         and a polymerase with reverse transcriptase activity, said         polymerase further comprising a mutation conferring an improved         nucleic acid extension rate and/or an improved reverse         transcriptase activity relative to the respective wildtype         polymerase.

An “analytical system” is an arrangement of components such as instruments interacting with each other with the ultimate aim to analyze a given sample.

The analytical system (440, FIG. 11) of the present invention is a system (440) comprising a module (401) for isolating and/or purifying an analyte. Further, the system (440) additionally comprises a module (403) for analyzing said analyte to obtain a detectable signal. The detectable signal can be detected in the same module (401, 402, 403) or, alternatively, in a separate module. The term “module” as used herein relates to any spatially defined location within the analyzer (400). Two modules (401, 403) can be separated by walls, or can be in open relationship. Any one module (401, 402, 403) can be either autonomously controlled, or control of the module (401, 402, 403) can be shared with other modules. For example, all modules are controlled centrally. Transfer between modules (401, 402, 403) can be manual, but can be automated. Thus, a number of different embodiments of automated analyzers (400) are encompassed by the present invention.

The “separation station” is described supra.

An “amplification station” comprises a temperature-controlled incubator for incubating the contents of at least two reaction vessels. It further comprises a variety of reaction vessels like tubes or plates, in which a reaction for the analysis of the sample such as PCR takes place. The outer limits or walls of such vessels are chemically inert such that they do not interfere with the amplification reaction taking place within. For the ease of handling and to facilitate automation, the at least two reaction vessels can be combined in an integral arrangement, so they can be manipulated together.

Consequently, an aspect of the invention is the analytical system described above, wherein the at least two reaction vessels are combined in an integral arrangement.

Integral arrangements can e.g. be vials or tubes reversibly or irreversibly attached to each other or arranged in a rack. For example, the integral arrangement is a multiwell plate.

For example, said multiwell plate is held in a holding station. In an embodiment, one handler transports a multiwell vessel from a holding station to an air-lock (460), and a second handler transports said multiwell plate from said air-lock to said amplification station, wherein both handlers interact with said multiwell plate by a form-locking interaction.

In an embodiment, the analytical system is fully automated.

In one embodiment, at least two reaction vessels combined in an integral arrangement are transported between stations of the system.

In a second embodiment, the purified target nucleic acid is transferred from said separation station to said amplification station. For example, a pipettor comprising pipets with attached pipet tips transfers the liquid comprising the purified nucleic acid.

In a third embodiment, the purified nucleic acid is transferred from said separation station to a reaction vessel in an integral arrangement held in a holding station. For example, said reaction vessel in an integral arrangement is then transferred from said holding station to said amplification station.

The analytical system according to the invention may further comprises a pipetting unit. Said pipetting unit comprises at least one pipet, or multiple pipets. In an embodiment, said multiple pipets are combined in one or more integral arrangements, within which the pipets can be manipulated individually. Pipets used in the context of the invention can be pipets comprising pipet tips as described supra. In another embodiment, the pipets are pipetting needles.

Alternatively, a reaction vessel or arrangement of reaction vessels used for sample preparation in the separation station and containing the fluid comprising the purified target nucleic acids may be transferred from the separation station to the amplification station.

For this purpose, the analytical system according to the invention may further comprises a transfer unit, said transfer unit comprising a robotic device, said device may comprise a handler.

For the reasons set out above in the context of the process according to the invention, the following are further aspects of the invention:

-   -   The analytical system (440) described above wherein at least one         reaction vessel comprises an RNA target nucleic acid and a DNA         target nucleic acid.     -   The analytical system (440) described above, wherein at least         one reaction vessel comprises an RNA target nucleic acid, and at         least one other reaction vessel comprises a DNA target nucleic         acid.

For example, the analytical system (440) described above further comprises one or more elements selected from the group consisting of:

-   -   a detection module (403) for detecting signals evoked by an         analyte     -   a sealer (410)     -   a storage module (1008) for reagents and/or disposables.     -   a control unit (1006) for controlling system components.

A “detection module” (403) can e.g. be an optical detection unit for detecting the result or the effect of the amplification procedure. An optical detection unit may comprise a light source, e.g. a xenon lamp, optics such as mirrors, lenses, optical filters, fiber optics for guiding and filtering the light, one or more reference channels, or a CCD camera or a different camera.

A “sealer” (410) is constructed and arranged to seal any vessels used in connection with the analytical system according to the invention. Such a sealer can, for example, seal tubes with appropriate caps, or multiwell plates with foil, or other suitable sealing materials.

A “storage module” (1008) stores the necessary reagents to bring about a chemical or biological reaction important for analysis of the fluid sample. It can also comprise further components useful for the method of the invention, e.g. disposables such as pipet tips or vessels to be used as reaction vessels within the separation station and/or the amplification station.

For example, the analytical system according to the invention further comprises a control unit for controlling system components.

Such a “control unit” (1006) may comprise software for ensuring that the different components of said analytical system work and interact correctly and with the correct timing, e.g. moving and manipulating components such as pipets in a coordinated manner. The control unit may also comprise a processor running a real-time operating system (RTOS), which is a multi-tasking operating system intended for real-time applications. In other words the system processor is capable of managing real-time constraints, i.e. operational deadlines from event to system response regardless of system load. It controls in real time that different units within the system operate and respond correctly according to given instructions.

In an embodiment, the present invention relates to an analytical system (440) for processing an analyte, comprising

a. a first position comprising first receptacles (1001) in linear arrangement comprising liquid samples (1010), a processing plate (101) comprising receptacles (103) in n×m arrangement for holding a liquid sample (1011), a first pipetting device (700) comprising at least two pipetting units (702) in linear arrangement, wherein said pipetting units (702) are coupled to pipette tips (3, 4), and a tip rack (70) comprising pipette tips (3, 4) in an a×(n×m) arrangement; b. a second position comprising a holder (201, 128) for said processing plate (101), a holder (330) for a multiwell plate, a holder (470) for said tip rack (70) and a second pipetting device (35), said second pipetting device (35) comprising pipetting units (702) in an n×m arrangement for coupling to pipette tips (3, 4) (FIG. 12). The term “holder” as used herein relates to any arrangement capable of receiving a rack or a processing plate.

The advantages of the analytical system (440) of the present invention are as described above for the method of the present invention.

For example the position of said pipetting units (702) of the first pipetting device (700) are variable. Embodiments of said first pipetting device (700) are described hereinafter.

In one embodiment, the tip rack (70) comprises pipette tips (3, 4) in an a×(n×m) arrangement. For example, a first type (4) and a second type (3) of pipette tips are comprised in the tip rack (70). In this embodiment, the first type of pipette tips (4) is arranged in an n×m arrangement, and the second type of pipette tips (3) is arranged in the n×m arrangement. In this context, “n” denotes the number of rows and m the number of columns, wherein n can be 6 and m is 8. For example, the first type of pipette tips (4) has a different volume than the second type of pipette tips (3), or the volume of the first type of pipette tips (4) is more than 500 ul, and the volume of the second type of pipette tips (3) is less than 500 ul. In this embodiment, a=2. However, embodiments of the invention with more than two types of pipette tips, and thus a >2 are also included in the present invention.

In one aspect, the analytical system (440) of the present invention comprises a control unit (1006) for allocating sample types and individual tests to individual positions of said processing plate (101). For example, said positions are separate cells (401, 402).

In one aspect of the invention, the system additionally comprises a transfer system (480) for transferring said process plate (101) and said rack (70) between first (402) and second (401) positions. Embodiments of said transfer system (480) are conveyor belts or, one or more handler.

Furthermore, said pipette units of said second pipetting device (35) may be engaged to pipette tips (3, 4) which were used in the first position (402).

An embodiment of the system (440) of the present invention additionally comprises a third station (403) comprising a temperature-controlled incubator for incubating said analyte with reagents necessary to obtain a detectable signal. Further embodiments of this system are described hereinafter.

More optimal control of the allocation of samples and tests to the n×m arrangement is achieved with a first processor (1004) which is comprised in said first position (402) to which said control unit (1006) transfers instructions for allocating sample types and individual tests to specific positions in the n×m arrangement of vessels (103) of the process plate (101), and a second processor (1005) which is comprised in said second position (401) to which said control unit (1006) transfers instructions for allocating sample types and individual tests to specific positions in the n×m arrangement of vessels (103) of the process plate.

For example, said system additionally comprises a first processor located in said first position, and a second processor located in said second position.

For example, said first processor (1004) controls said first pipetting device (700) and said second processor (1005) controls said second pipetting device (35).

All other embodiments and specific descriptions of embodiments of the analytical system according to the invention are those mentioned for the process according to the invention.

DESCRIPTION OF THE FIGURES

FIG. 1:

Schematic depiction of the sample preparation workflow as used in an embodiment of the invention.

Arrows pointing down denote addition of a component or reagent to each respective well of the deepwell plate mentioned above, arrows pointing up their respective removal. These actions were performed manually in steps 2, 3, 4, 21 and 22, by the process head of the apparatus in steps 10, 14, 16, 18, and 24, and by the reagent head of the apparatus in steps 5, 6, 7, 11, 15 and 19.

It has to be understood that the volumes used can be adjusted flexibly within the spirit of the invention, for example at least about up to 30% of the disclosed values. In particular, in the case of step 2, the sample volume can be variable in order to take into account the different types of fluid samples which may require more or less starting material for obtaining proper results, as known by the artisan. For example, the range is from about 100 ul to about 850 ul. For example, it is about 100 ul, about 500 ul or about 850 ul. For example, the volume in the respective vessels is adjusted to an identical total volume with the diluent in step 3. For example, as in the scheme shown in FIG. 1, the total volume adds up to about 850 ul.

FIG. 2:

Growth curves of the amplifications of the target nucleic acids derived from HIV, HBV and CT carried out on a LightCycler480 (Roche Diagnostics GmbH, Mannheim, Del.) as described in Example 1. The “Signal” indicated on the y-axis is a normalized fluorescent signal. The x-axis shows the number of the respective PCR cycle.

The growth curves of HIV and HBV are shown along with the growth curves of the corresponding internal control nucleic acid. The respective target nucleic acid curves are represented by straight lines, the control nucleic acid curves by dotted lines.

FIG. 2a : Qualitative HIV assay, measured in the channel for detection of the target probe.

FIG. 2b : Qualitative HIV assay, measured in the channel for detection of the control probe.

FIG. 2c : Quantitative HIV assay, measured in the channel for detection of the target probe.

FIG. 2d : Quantitative HIV assay, measured in the channel for detection of the control probe.

FIG. 2e : Quantitative HBV assay, measured in the channel for detection of the target probe.

FIG. 2f : Quantitative HBV assay, measured in the channel for detection of the control probe.

FIG. 2g : CT assay, measured in the channel for detection of the target probe.

FIG. 3:

Perspective view of the processing plate.

FIG. 4:

Perspective view of the processing plate from the opposite angle.

FIG. 5:

Top view of the processing plate.

FIG. 6:

Cross-sectional view along the longer side of the processing plate.

FIG. 7:

A partial view of the cross-sectional view.

FIG. 8:

Perspective view of the longer side of the processing plate.

FIG. 9:

a) to d) show different views of the second embodiment of the magnetic separation station.

FIG. 10:

(a) to (c) show a view of the first embodiment of the magnetic separation station holding the Processing plate, with the first type of magnets in the uppermost Z-position, and the second type of magnets in the lowermost Z-position.

FIG. 11:

Schematic drawings of an analyzer comprising different stations, modules or cells.

FIG. 12:

Shows an analytical system of the present invention.

FIG. 13:

Linearity of the quantitative HBV assay in EDTA plasma according to the data in Example 2.

FIG. 14:

Linearity of the quantitative HBV assay in serum according to the data in Example 2.

FIG. 15:

Linearity of the quantitative HCV assay in EDTA plasma according to the data in Example 2.

FIG. 16:

Linearity of the quantitative HCV assay in serum according to the data in Example 2.

FIG. 17:

Linearity of the quantitative HIV assay in EDTA plasma according to the data in Example 2.

EXAMPLES

The following examples are offered to illustrate, but not to limit the claimed invention.

Example 1

This example describes a process for isolating and simultaneously amplifying at least a first and a second target nucleic acid using a single generic internal control nucleic acid.

In brief, in the depicted embodiment, realtime PCR is carried out simultaneously and under identical conditions on a panel of several different targets comprising bacteria (Chlamydia trachomatis, CT) as well as a DNA virus (HBV) and an RNA virus (HIV). All samples were processed and analyzed within the same experiment, i.e. on the same deepwell plate (for sample preparation) or multiwell plate (for amplification and detection), respectively.

The following samples were prepared and subsequently analyzed:

Reagent Manufacturer: HIV-1M Secondary Standard, 50000 Roche cp/ML HBV Secondary Standard, 400 IU/ml Roche CT (DNA POS CTL pCHL-1) Roche

Suitable standards or other types of targets are available to the skilled artisan.

The instruments listed in the following table were used according to the instructions of the respective manufacturer:

Instrument Manufacturer Hamilton Star Hamilton Medical AG (Bonaduz, CH) Light Cycler 480 Roche Diagnostics GmbH (Mannheim, DE) Chameleon Sealer K biosystems (Essex, UK) Compressor K biosystems (Essex, UK)

For sample preparation the following reagents were used as diluents:

Reagent Manufacturer: PreservCyt Thin Prep K3 EDTA Plasma, PCR neg. Roche

The following dilutions were prepared in advance and stored overnight (plasma dilutions at −60 to −90° C., PreservCyt dilutions at 2-8° C.):

Target Concentration Matrix HBV 50 IU/ml K3 EDTA plasma HIV-1M 100 cp/ml K3 EDTA plasma CT 2.5 fg/ml PreservCyt

Each respective sample (500 ul) and each respective specimen diluent (350 ul) were pipetted manually into a deepwell plate, wherein each sample was added to three different wells for triplicate analysis. To each well containing an HIV or HBV sample, 50 ul of an internal control nucleic acid were manually added. For the qualitative HIV assay, an RNA serving as a qualitative control was added (100 armored particles/sample). For the quantitative HIV assay, an RNA serving as a quantitative standard was added (500 armored particles/sample). For the quantitative HBV assay, a DNA serving as a quantitative standard was added (1E4 copies/sample). The sequence of said control nucleic acids was identical in all cases and selected from the group of SEQ ID NOs 45-48.

The respective control nucleic acid was stored in the following buffer:

IC/IQS - Storage Buffer Conc. or pH Tris (mM) 10 EDTA (mM) 0.1 Sodium Azide (w/v, %) 0.05 Poly rA RNA (mg/l) 20 pH 8

Sample preparation was performed on a Hamilton Star (Hamilton, Bonaduz, CH), following the workflow according to the scheme depicted in FIG. 1 and using the following reagents:

Protease reagent Conc. or pH Tris (mM) 10 EDTA (mM) 1 Calcium Chloride (mM) 5 Calcium Acetate (mM) 5 Esperase (mg/ml) 80 Glycerin (w/v, %) 50 pH 5.5

MGP Reagent Conc. or pH MPG Powder (mg/ml) 60 Tris (mM) 30 Methylparaben (w/v, %) 0.1 Sodium Azide (w/v, %) 0.095 pH 8.5

Lysis Reagent Conc. or pH Guanidine Thiocyanate (M) 4 Sodium Citrate (mM) 50 Polydocanol (w/v, %) 5 Dithiotreitol (w/v, %) 2 pH 5.8

Wash buffer Conc. or pH Sodium Citrate (mM) 7.5 Methylparaben (w/v, %) 0.1 pH 4.1

Elution buffer Conc. or pH Tris (mM) 30 Methylparaben (w/v, %) 0.2 pH 8.5

After the final step, the process head of the Hamilton Star apparatus added the respective mastermixes (Mmxs) containing amplification reagents to each well, mixed the fluids containing the isolated nucleic acids with the Mmx and transferred each resulting mixture to a corresponding well of a microwell plate in which the amplification was carried out.

The following mastermixes (each consisting of the two reagents R1 and R2) were used:

For HIV:

Concentration/50 R1 Reagent μl-PCR [μM] Water (PCR grade) Mn(Ac)₂* 4H₂O (pH 6.1 adjusted with 3′000 Acetic Acid) NaN3/Ri, buffered with 10 mM Tris at pH7 [%] 0.018 Concentration/50 R2 Reagent μl-PCR [μM] DMSO [%] 5.000% NaN3/Ri, buffered with 10 mM Tris at pH7 [%] 0.027% Potassium acetate pH 7.0 110′000 Glycerol [%] 3.000% Tricine pH 8.0 50′000 Igepal [%] 0.024% dGTP 337.5 dATP 337.5 dCTP 337.5 dUTP 675 Primers/probes selected from SEQ ID NOs 1-35 0.1-0.15 SEQ ID NO 42 0.1 SEQ ID NO 43 0.1 SEQ ID NO 44 0.1 Uracil-N-Glycosylase 10 (U/reaction) Z05-D Polymerase 40 (U/reactionn) NTQ21-46A - Aptamer 0.222 Water

For HBV:

R2 Reagent Concentration/50 μl-PCR H2O 100 % Tricine 7.7 40 mM Tween 0.03 % (v/v) Glycerol 5 % (v/v) KOH 25.2 mM KOAc 121.8 mM NTQ21-46A (Aptamer) 0.2625 uM dGTP 0.42 uM dATP 0.42 uM dCTP 0.42 uM dUTP 0.84 uM SEQ ID NO 36 1.2 uM SEQ ID NO 37 0.1 uM SEQ ID NO 38 1.2 uM SEQ ID NO 42 0.6 uM SEQ ID NO 43 0.6 uM SEQ ID NO 44 0.15 uM ZO5D Polymerase 35 (U/reaction) Uracil-N-Glycosylase 2 (U/reaction) Sodium Azide 0.027 % (m/v) R1 Reagent Concentration/50 μl-PCR H2O 100 % MgOAc 2.5 mM MnOAc pH 6.1 2.5 mM Sodium Azide 0.018 % (m/v)

For CT:

R1 Reagent Concentration/50 μl-PCR Water (PCR grade) Mn(Ac)₂ (pH 6.5 in 0.002% (VN) Glacial 2.7 mM Acetic Acid) NaN3 0.0135% (W/V) R2 Reagent Concentration/50 μl-PCR NaN3/Ri, buffered with 10 mM Tris at 0.0315 % pH7 [%] Potassium acetate 112.4 mM Glycerol [%] 3.5 % Tricine 61 mM Potassium hydroxide 28.4 mM dGTP 525 uM dATP 525 uM dCTP 525 uM dUTP 1.05 mM SEQ ID NO 39 750 nM SEQ ID NO 40 600 nM SEQ ID NO 41 116 nM Aptamer NTQ-46A 175 nM Uracil-N-Glycosylase 5 U/reaction Z05-D Polymerase 31 U/reaction

For amplification and detection, the microwell plate was sealed with an automated plate sealer (see above), and the plate was transferred to a LightCycler 480 (see above).

The following PCR profile was used:

Thermo cycling profile Program Target Acquisition Hold Ramp Rate Analysis Name (° C.) Mode (hh:mm:ss) (° C./s) Cycles Mode Pre-PCR 50 None 00:02:00 4.4 1 None 94 None 00:00:05 4.4 55 None 00:02:00 2.2 60 None 00:06:00 4.4 65 None 00:04:00 4.4 1st 95 None 00:00:05 4.4 5 Quantification Measurement 55 Single 00:00:30 2.2 2nd 91 None 00:00:05 4.4 45 Quantification Measurment 58 Single 00:00:25 .2 Cooling 40 None 00:02:00 2.2 1 None

Filter Combination Integration Time (sec) 435-470 1 495-525 0.5 540-580 0.5 610-645 0.5 680-700 1

The Pre-PCR program comprises initial denaturing and incubation at 55, 60 and 65° C. for reverse transcription of RNA templates. Incubating at three temperatures combines the advantageous effects that at lower temperatures slightly mismatched target sequences (such as genetic variants of an organism) are also transcribed, while at higher temperatures the formation of RNA secondary structures is suppressed, thus leading to a more efficient transcription.

PCR cycling is divided into two measurements, wherein both measurements apply a one-step setup (combining annealing and extension). The first 5 cycles at 55° C. allow for an increased inclusivity by pre-amplifying slightly mismatched target sequences, whereas the 45 cycles of the second measurement provide for an increased specificity by using an annealing/extension temperature of 58° C.

Using this profile on all samples comprised on the microwell plate mentioned above, amplification and detection was achieved in all samples, as depicted in FIG. 2. This shows that the sample preparation prior to amplification was also successfully carried out.

The results for the qualitative and quantitative HIV internal controls and the quantitative HBV internal control are depicted separately in FIG. 2 for the sake of clarity. It can be seen that the controls were also successfully amplified in all cases. The quantitation of the HIV and HBV targets in the quantitative setup were calculated by comparison with the internal control nucleic acid serving as a quantitative standard.

Example 2

The generic amplification process described hereinabove was carried out on a variety of different target nucleic acids in separate experiments but under identical conditions. Isolation of the respective nucleic acid was carried out as described under Example 1.

The respective generic internal control nucleic acid was selected from SEQ ID NOs 45-49 and was armored RNA for RNA targets and lambda-packaged DNA for DNA targets. For qualitative RNA assays, 300 particles were added per sample, for quantitative RNA assays 3000 and for all DNA assays 500.

The following PCR profile was used on all targets:

Target Acquisition Plateau Measure Ramp Rate [° C.] Mode [hh:mm:ss] [hh:mm:ss] [° C./s] Pre- UNG-Step 50 none 00:02:00 00:00:00 2.2 PCR UNG/Template 94 none 00:00:05 00:00:00 4.4 Denaturation RT-Step 55 none 00:02:00 00:00:00 2.2 60 none 00:06:00 00:00:00 4.4 65 none 00:04:00 00:00:00 4.4 1st Measurement 95 none 00:00:05 00:00:00 4.4 55 single 00:00:30 00:00:08 2.2 2nd Measurement 91 none 00:00:05 00:00:00 4.4 58 single 00:00:25 00:00:08 2.2 Cooling 40 none 00:02:00 00:00:00 2.2

Name Cycles Pre-PCR 1 1st Measurement 5 2nd 45 Measurement Cooling 1

In detail, the following experiments were performed:

1. Qualitative multiplex analysis of HBV, HCV and HIV

-   -   a. Mastermix

R1:

Conc. In 50 ul-PCR (uM) Mn(Ac)2 * 4H2O (pH 6.1 adjusted 3′300 with Acetic Acid) NaN3/Ri, buffered with 10 mM Tris at pH7 0.018 pH: 6.41

R2:

Reagent Conc. in 50 ul-PCR (uM) DMSO (%) 5.4 NaN3/Ri, buffered with 10 mM Tris at pH7 0.027 KOAc (pH 7.0) 120′000 Glycerol (%) 3 Tween 20(%) 0.015 Tricine pH 8.0 60000 NTQ21-46A - Aptamer 0.2222 Uracil-N-Glycosylase (U/uL) 0.2 dGTP 400.0 dATP 400.0 dCTP 400.0 dUTP 800.0 ZO5-D Polymerase (U/ul)* .09 Primers/probes selected from SEQ ID NOs 1-35 0.125-0.3 SEQ ID NO 36 0.100 SEQ ID NO 37 0.100 SEQ ID NO 38 0.150 Primers/probes selected from SEQ ID NOs 60-76 0.050-0.250 SEQ ID NO 42 0.200 SEQ ID NO 43 0.200 SEQ ID NO 44 0.100

Analytical Sensitivity/LOD

For each detected virus (HIV-1 group M, HIV-1 group 0, HIV-2, HBV and HCV), at several concentrations/levels at and around the anticipated LOD for EDTA-plasma. One panel per virus and concentration was tested with at least 20 valid replicates per concentration. The LOD was determined by PROBIT analysis (see Table 1-5).

HIV

TABLE 1 HIV-1 Group M Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 32 cp/mL 21 21 100% 16 cp/mL 21 21 100%  8 cp/mL 21 21 100%  4 cp/mL 21 20  95%  2 cp/mL 21 15  71%  1 cp/mL 21 9  43%  0 cp/mL (neg. control) 12 0  0% LOD by PROBIT analysis (95% hitrate) 4.06 cp/mL 95% confidence interval for LOD by PROBIT analysis 2.85-9.24 cp/mL

Titer of WHO Standard for HIV-1 Group M was converted to IU/mL.

${{Titer}\left( {{in}\frac{IU}{mL}} \right)} = \frac{{Titer}\left( {{in}\frac{cp}{mL}} \right)}{0.6}$

Therefore HIV-1 Group M LOD in IU/mL is

LOD by PROBIT analysis (95% hitrate): 6.77 IU/mL

95% confidence interval for LOD by PROBIT analysis: 4.75-15.4 IU/mL

TABLE 2 HIV-1 Group O Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 60 cp/mL 21 21 100% 30 cp/mL 20 20 100% 20 cp/mL 21 21 100% 14 cp/mL 21 19  90% 7 cp/mL 21 15  71% 4.5 cp/mL 21 12  57% 0 cp/mL 12 0  0% (neg. control) LOD by PROBIT analysis 14.9 cp/mL (95% hitrate) 95% confidence interval for 10.9-31.5 cp/mL LOD by PROBIT analysis

Titer of Primary Standard for HIV-1 Group 0 was reassigned to CBER HIV-1 Group 0 panel; calculation factor is 0.586.

Therefore HIV-1 Group 0 LOD is

LOD by PROBIT analysis (95% hitrate): 8.8 cp/mL

95% confidence interval for LOD by PROBIT analysis: 6.4-18.5 cp/mL

TABLE 3 HIV-2 Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 4 cp/mL 21 21 100% 2 cp/mL 21 21 100% 1 cp/mL 21 20  95% 0.5 cp/mL 21 13  62% 0.25 cp/mL 21 13  62% 0.125 cp/mL 21 7  33% 0 cp/mL 12 0  0% (neg. control) LOD by PROBIT analysis 1.29 cp/mL (95% hitrate) 95% confidence interval for −3.11 cp/mL LOD by PROBIT analysis

Titer of Primary Standard for HIV-2 was reassigned to CBER HIV-2 panel; calculation factor is 26.7.

Therefore HIV-2 LOD is

LOD by PROBIT analysis (95% hitrate): 34.44 cp/mL 95% confidence interval for LOD by PROBIT analysis: 21.89-83.04 cp/mL

HBV

TABLE 4 HBV Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 7.6 IU/mL 21 21 100% 3.8 IU/mL 21 21 100% 1.9 IU/mL 21 20  95% 0.95 IU/mL 21 14  67% 0.6 IU/mL 19 12  63% 0.4 IU/mL 21 12  57% 0 IU/mL 12 0  0% (neg. control) LOD by PROBIT analysis 2.27 IU/mL (95% hitrate) 95% confidence interval for 1.48-6.54 IU/mL LOD by PROBIT analysis

HCV

TABLE 5 HCV Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 24 IU/mL 21 21 100% 12 IU/mL 21 21 100% 6 IU/mL 21 21 100% 3 IU/mL 21 17  81% 1.5 IU/mL 21 14  67% 0.75 IU/mL 21 9  43% 0 IU/mL 18 0  0% (neg. control) LOD by PROBIT analysis 4.76 IU/mL (95% hitrate) 95% confidence interval for 3.14-11.61 IU/mL LOD by PROBIT analysis

2. Qualitative analysis of WNV

Mastermix

R1:

Reagent Conc. in 50 ul-PCR (uM) Mn(Ac)2 * 4H2O (pH 6.1 adjusted 3'300 with Acetic Acid) NaN3/Ri, buffered with 10 mM 0.018 Tris at pH 7 pH: 6.41

R2:

Reagent Conc. in 50 ul-PCR (uM) DMSO (%) 5.4 NaN3/Ri, buffered with 10 mM  0.027 Tris at pH 7 K acetate pH 7.0 120'000      Glycerol (%) 3   Tween 20 (%)   0.015 Tricine pH 8.0 60'000      NTQ21-46A-Aptamer   0.2222 Uracil-N-Glycosylase (U/uL) 0.2 dGTP 400.0  dATP 400.0  dCTP 400.0  dUTP 800.0  ZO5-D Polymerase (U/ul)* 0.9 Primers/probes selected from 0.08-0.4  SEQ ID NOs 53-59 SEQ ID NO 42  0.150 SEQ ID NO 43  0.150 SEQ ID NO 44  0.100

Analytical Sensitivity/LOD

For the viruses (WNV, SLEV and JEV) an independent panel was prepared as a dilution series of the respective Standard including several concentrations/levels at and around the anticipated LOD. One panel per virus and concentration was tested with at least 20 valid replicates per concentration.

The LOD was determined by PROBIT analysis.

TABLE 6 WNV Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 20 cp/mL 21 21  100% 12 cp/mL 21 21  100% 8 cp/mL 21 21  100% 5 cp/mL 21 17   81% 2.5 cp/mL 21 15 71.4% 0.5 cp/mL 21 1  4.8% 0 cp/mL 12 0   0% (neg. control) LOD by PROBIT analysis 6.57 cp/mL (95% hitrate) 95% confidence interval for 4.74-11.03 cp/mL LOD by PROBIT analysis

TABLE 7 SLEV Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 140 cp/mL 21 21  100% 100 cp/mL 21 20 95.2% 70 cp/mL 21 20 95.2% 40 cp/mL 21 17 81.0% 20 cp/mL 21 11 52.4% 10 cp/mL 21 6 28.6% 0 cp/mL 12 0   0% (neg. control) LOD by PROBIT analysis 78.9 cp/mL (95% hitrate) 95% confidence interval for 55.4-145.7 cp/mL LOD by PROBIT analysis

TABLE 8 JEV Hit rates and Probit LOD from individual panel Number of Number of Concentration replicates positives Hit rate 20 cp/mL 21 20 95.2% 12 cp/mL 21 20 95.2% 8 cp/mL 21 18 85.7% 5 cp/mL 21 17 81.0% 2.5 cp/mL 21 14 66.7% 0.5 cp/mL 21 2 9.52% 0 cp/mL 12 0   0% (neg. control) LOD by PROBIT analysis 13.55 cp/mL (95% hitrate) 95% confidence interval for 8.78-27.7 cp/mL LOD by PROBIT analysis

3. Quantitative analysis of HBV

Mastermix

R1:

Reagent Final Conc. in 50 ul-PCR (uM) Mn(Ac)2 * 4H2O (pH 6.1 adjusted 3'300 with Acetic Acid) NaN3/Ri, buffered with 10 mM 0.018 Tris at pH 7 pH: 6.41

R2:

Reagent Final Conc. in 50 ul-PCR (uM) Glycerol (%, w/v)    3% Tricine 60 mM DMSO (%, v/v)  5.4% KOAc 120 mM Tween 20 (v/v) 0.015% Aptamer NTQ21-46 A 0.222 μM ZO5D Polymerase 0.9 U/μL (45 U/rxn) Uracil-N-Glycosylase 0.2 U/μL (10 U/rxn) Sodium Azide (w/v) 0.027% dCTPs 400 μM dGTPs 400 μM dATPs 400 μM dUTPs 800 μM SEQ ID NO 36 1.2 μM SEQ ID NO 37 1.2 μM SEQ ID NO 50 0.6 μM SEQ ID NO 51 0.6 μM SEQ ID NO 38 0.1 μM SEQ ID NO 52 M

Analytical Sensitivity/LOD

Four dilution panels were prepared with HBV Secondary Standard (representing Genotype A), i.e., two in HBV negative serum for sample input volumes of 200 μL and 500 μL, and two in HBV negative EDTA-plasma for sample input volumes of 200 μL and 500 μL. Each panel included 7 concentration levels at and around the anticipated LOD. One panel per matrix was tested with >21 replicates per concentration level. At least 20 replicates needed to be valid. The LOD was determined by PROBIT analysis at 95% hit rate and by >95% hit rate analysis.

TABLE 9 LOD analysis for 200 μL input volume in EDTA-plasma. * Number of Number of Concentration replicates positives Hit rate 25 IU/mL 41 41  100% 15 IU/mL 41 39 95.1% 10 IU/mL 41 40 97.6% 7 IU/mL 41 40 97.6% 4 IU/mL 24 20 83.3% 1 IU/mL 24 4 16.7% 0 IU/mL 24 0   0% (neg. control) LOD by PROBIT analysis 8.2 IU/mL (95% hitrate) 95% confidence interval for 4.8-26.0 IU/mL LOD by PROBIT analysis * Additional replicates were tested to narrow the observed 95% confidence interval.

TABLE 10 LOD analysis for 500 μL input volume in EDTA-plasma. Number of Number of Concentration replicates positives Hit rate 10 IU/mL 21 21  100% 7 IU/mL 21 21  100% 4 IU/mL 21 21  100% 2.5 IU/mL 21 20 95.2% 1 IU/mL 21 14 66.7% 0.2 IU/mL 21 1  4.8% 0 IU/mL 21 0   0% (neg. control) LOD by PROBIT analysis 2.3 IU/mL (95% hitrate) 95% confidence interval for 1.6-4.2 IU/mL LOD by PROBIT analysis

TABLE 11 LOD analysis for 200 μL input volume in serum. Number of Number of Concentration replicates positives Hit rate 25 IU/mL 21 21  100% 15 IU/mL 21 20 95.2% 10 IU/mL 21 21  100% 7 IU/mL 21 20 95.2% 4 IU/mL 21 15 71.4% 1 IU/mL 21 8 38.1% 0 IU/mL 21 0   0% (neg. control) LOD by PROBIT analysis 9.4 IU/mL (95% hitrate) 95% confidence interval for 6.2-19.0 IU/mL LOD by PROBIT analysis

TABLE 12 LOD analysis for 500 μL input volume in serum. Number of Number of Concentration replicates positives Hit rate 10 IU/mL 21 21  100% 7 IU/mL 21 21  100% 4 IU/mL 21 21  100% 2.5 IU/mL 21 16 76.2% 1 IU/mL 21 16 76.2% 0.2 IU/mL 21 7 33.3% 0 IU/mL 21 0   0% (neg. control) LOD by PROBIT analysis 4.1 IU/mL (95% hitrate) 95% confidence interval for 2.4-10.0 IU/mL LOD by PROBIT analysis

Summary LOD:

EDTA-plasma: The PROBIT analysis at 95% hit rate resulted in an LOD of 8.2 IU/mL for 200 μL sample input volume and 2.3 IU/mL for 500 μL sample input volume for EDTA-plasma.

The 95% confidence interval range for these concentrations was 4.8-26.0 IU/mL for 200 μL sample input volume and 1.6-4.2 IU/mL for 500 μL sample input volume.

Serum: The PROBIT analysis at 95% hit rate resulted in an LOD of 9.02 IU/mL for 200 μL sample input volume and 4.1 IU/mL for 500 μL sample input volume for serum.

The 95% confidence interval range for these concentrations was 6.2-19.0 IU/mL for 200 μL sample input volume and 2.4-10.0 IU/mL for 500 μL sample input volume.

Linearity

One EDTA-plasma panel and one serum panel were prepared by using HBV genotype A (provided by RMD Research Pleasanton, linearized plasmid, pHBV-PC ADW2). Each of the panels was analyzed at 12 concentration levels for the determination of the expected dynamic range (4-2E+09 IU/mL) of the assay. All concentration levels/panel members (PM) were tested in 21 replicates.

This study was done with a sample input volume of 500 μL. The concentration levels were selected as follows: One level below expected Lower Limit of Quantitation (LLOQ), one at expected LLOQ, one above expected LLOQ, several concentrations at intermediates levels, at expected Upper Limit of Quantitation (ULOQ) and one above expected ULOQ:

PM 12—2.0E+09 IU/mL—above expected ULOQ

PM 11—1.0E+09 IU/mL—at expected ULOQ

PM 10—1.0E+08 IU/mL—below expected ULOQ

PM 9—1.0E+07 IU/mL—intermediate concentration level

PM 8—1.0E+06 IU/mL—intermediate concentration level

PM 7—1.0E+05 IU/mL—intermediate concentration level

PM 6—1.0E+04 IU/mL—intermediate concentration level

PM 5—1.0E+03 IU/mL—intermediate concentration level

PM 6a—2.0E+02 IU/mL—intermediate concentration level (PM 6 diluted to 2.0E+02 IU/mL, used for titer assignment of serum panel)

PM 4—1.0E+02 IU/mL—intermediate concentration level (also used for titer assignment of plasma panel)

PM 3—5.0E+01 IU/mL—above expected LLOQ

PM 2—1.0E+01 IU/mL—at expected LLOQ

PM 1—4.0E+00 IU/mL below expected LLOQ

For every valid sample of the linearity panel, the observed HBV DNA titer was transformed to log 10 titer and the mean log 10 titer was calculated per concentration level.

TABLE 13 Linearity in EDTA Plasma Nominal Assigned Assigned Mean Log 10 Titer Titer Log10 Titer (IU/mL) (IU/mL) Titer observed Replicates 4.00E+00 3.50E+00 0.54 0.52 17 1.00E+01 8.70E+00 0.94 0.91 21 5.00E+01 4.40E+01 1.64 1.69 21 1.00E+02 8.70E+01 1.94 2.04 21 1.00E+03 8.70E+02 2.94 3.01 21 1.00E+04 8.70E+03 3.94 3.9 21 1.00E+05 8.70E+04 4.94 4.88 21 1.00E+06 8.70E+05 5.94 5.87 21 1.00E+07 8.70E+06 6.94 6.92 21 1.00E+08 8.70E+07 7.94 8.01 21 1.00E+09 8.70E+08 8.94 9.04 21 2.00E+09 1.70E+09 9.24 9.38 21

A graphical depiction of this result is shown in FIG. 13.

TABLE 14 Linearity in Serum Nominal Assigned Assigned Mean Log 10 Titer Titer Log10 Titer (IU/mL) (IU/mL) Titer observed Replicates 4.00E+00 3.30E+00 0.52 0.7 21 1.00E+01 8.30E+00 0.92 0.99 21 5.00E+01 4.10E+01 1.62 1.73 21 1.00E+02 8.30E+01 1.92 2.03 21 1.00E+03 8.30E+02 2.92 2.93 21 1.00E+04 8.30E+03 3.92 3.8 21 1.00E+05 8.30E+04 4.92 4.78 21 1.00E+06 8.30E+05 5.92 5.75 21 1.00E+07 8.30E+06 6.92 6.73 21 1.00E+08 8.30E+07 7.92 7.78 21 1.00E+09 8.30E+08 8.92 8.92 21 2.00E+09 1.70E+09 9.22 9.22 21

A graphical depiction of this result is shown in FIG. 14.

Summary Linearity:

The linear range, defined as the concentration range for which the log 10 deviation of the mean log 10 observed titers is within ±0.3 of the log 10 nominal titer was determined as: 3.5E+00 IU/mL-1.7E+09 IU/mL for EDTA-plasma and 3.3E+00 IU/mL-1.7E+09 IU/mL for serum. The Lower Limit of Quantitation was found to be: 4.0E+00 IU/mL for EDTA-plasma and serum.

4. Quantitative analysis of HCV

Mastermix

R1:

Final Conc. in 50 ul- Reagent PCR (uM) Mn(Ac)2 * 4H2O (pH 6.1 adjusted with Acetic Acid) 3′300 NaN3/Ri, buffered with 10 mM Tris at pH7 0.018 pH: 6.41

R2:

Final Conc. in Reagent 50 ul-PCR Glycerol (%, w/v)    3% Tricine  60 mM DMSO (%, v/v)  5.4% KOAc 120 mM Tween 20 (v/v) 0.015% NTQ21-46 A 0.222 μM ZO5D 0.9 U/μL (45 U/rxn) UNG 0.2 U/μL (10 U/rxn) Sodium Azide (w/v) 0.027    dCTPs   400 μM dGTPs   400 μM dATPs   400 μM dUTPs   800 μM Primers/probes selected from SEQ ID NOs  0.1 μM 60-76 SEQ ID NO 42  0.3 μM SEQ ID NO 43  0.3 μM SEQ ID NO 44 μM

Analytical Sensitivity/LOD

A dilution panel was prepared with Roche HCV Secondary Standard in HCV negative EDTA plasma and serum using a sample input volumes of 200 μL and 500 μL. Each concentration level was tested with 21 replicates. At least >20 replicates have to be valid. The LOD was determined by PROBIT analysis at 95% hit rate and by >95% hit rate analysis.

TABLE 15 Hit rates and Probit with 200 μL sample process input volume for EDTA-plasma Number of Number of Concentration replicates positives Hit rate   55 IU/mL 21 21 100%   38 IU/mL 21 21 100%   25 IU/mL 21 20  95% 12.5 IU/mL 21 19  90%   6 IU/mL 21 15  71%   3 IU/mL 21  6  29% 0 IU/mL (neg. control) 21  0  0% LOD by PROBIT analysis (95% hitrate) 17.4 IU/mL 95% confidence interval for LOD by PROBIT 12.1-34.3 analysis IU/mL

TABLE 16 Hit rates and Probit with 500 μL sample process input volume for EDTA-plasma Number of Number of Concentration replicates positives Hit rate  22 IU/mL 21 21 100%   15 IU/mL 21 21 100%   10 IU/mL 20 20 100%    5 IU/mL 21 19 76% 2.5 IU/mL 21 15 71%   1 IU/mL 21  6 57% 0 IU/mL (neg. control) 21  0  0% LOD by PROBIT analysis (95% hitrate) 9.0 IU/mL 95% confidence interval for LOD by PROBIT 5.5-25.4 analysis IU/mL

TABLE 17 Hit rates and Probit with 200 μL sample process input volume for serum Number of Number of Concentration replicates positives Hit rate  55 IU/mL 21 21 100%   38 IU/mL 21 21 100%   25 IU/mL 21 20 95% 12.5 IU/mL  21 18 86%   6 IU/mL 21 13 62%   3 IU/mL 21  6 29% 0 IU/mL (neg. control) 21  0  0% LOD by PROBIT analysis (95% hitrate) 20.2 IU/mL 95% confidence interval for LOD by PROBIT 14.0-39.3 analysis IU/mL

TABLE 18 Hit rates and Probit with 500 μL sample process input volume for serum Number of Number of Concentration replicates positives Hit rate 22 IU/mL 21 21 100%  15 IU/mL 21 21 100%  10 IU/mL 21 20 95%  5 IU/mL 21 18 86% 2.5 IU/mL  21 12 57%  1 IU/mL 21  4 19% 0 IU/mL (neg. control) 21  0  0% LOD by PROBIT analysis (95% hitrate) 8.2 IU/mL 95% confidence interval for LOD by 5.8-15.0 PROBIT analysis IU/mL

Summary LOD:

1. The PROBIT analysis at 95% Hit rate resulted in an LOD of 17.4 IU/mL for 200 μL sample process input volume and 9.0 IU/mL for 500 μL sample process input volume for EDTA plasma. The 95% confidence interval for these concentrations is 12.1-34.3 IU/mL for 200 μL sample process input volume and 5.5-25.4 IU/mL for 500 μL sample process input volume.

2. The values of the PROBIT analysis at 95% Hit rate is 20.2 IU/mL for 200 μL sample process input volume and 8.2 IU/mL for 500 μL sample process input volume for serum. The 95% confidence interval for these concentrations is 14.0-39.3 IU/mL for 200 μL sample process input volume and 5.8-15.0 IU/mL for 500 μL sample process input volume.

Linearity

One preparation of an EDTA-plasma panel and one preparation of a serum panel of HCV aRNA traceable to the HCV WHO Standard were analyzed. The linearity panels were prepared by serial dilution and analyzed at 10 different concentrations. The study was done with 500 μL sample process input volume. The concentrations were selected as follows: One level below expected Lower Limit of Quantification (LLoQ), one at LLoQ, one above LLOQ, several concentrations at intermediates levels, at expected Upper Limit of Quantification (ULoQ) and one at or above ULoQ. For all concentrations 21 replicates were tested.

PM 1—2.0E+08 IU/mL—above expected ULoQ

PM 2—1.0E+08 IU/mL—at expected ULoQ

PM 3—1.0E+07 IU/mL—below expected ULoQ

PM 4—1.0E+06 IU/mL—intermediate concentration level

PM 5 1.0E+05 IU/mL—intermediate concentration level

PM 6—1.0E+04 IU/mL—intermediate concentration level for titer assignment

PM 7—1.0E+03 IU/mL—intermediate concentration level

PM 8—1.0E+02 IU/mL—above expected LLoQ

PM 9—1.0E+01 IU/mL—at expected LLoQ

PM 10—8.0E+00 IU/mL—below expected LLoQ

TABLE 19 Linearity in EDTA Plasma Nominal Assigned Assigned Mean Log 10 Titer Titer Log10 Titer (IU/mL) (IU/mL) Titer observed Replicates 8.00E+00 4.87E+00 0.7 0.6 15 1.00E+01 6.09E+00 0.8 0.8 17 1.00E+02 6.09E+01 1.8 1.7 21 1.00E+03 6.09E+02 2.8 2.8 21 1.00E+04 6.09E+03 3.8 3.8 21 1.00E+05 6.09E+04 4.8 4.7 21/20 1.00E+06 6.09E+05 5.8 5.6 21/20 1.00E+07 6.09E+06 6.8 6.7 21 1.00E+08 6.09E+07 7.8 7.8/7.7 21/18 2.00E+08 1.22E+08 8.1 8   21/20

A graphical depiction of this result is shown in FIG. 15.

TABLE 20 Linearity in Serum Nominal Assigned Assigned Mean Log 10 Titer Titer Log10 Titer (IU/mL) (IU/mL) Titer observed Replicates 8.00E+00 3.90E+00 0.6 0.7 10 1.00E+01 4.96E+00 0.7 0.7 14 1.00E+02 4.96E+01 1.7 1.6 21 1.00E+03 4.96E+02 2.7 2.8 21 1.00E+04 4.96E+03 3.7 3.7 21 1.00E+05 4.96E+04 4.7 4.7 21 1.00E+06 4.96E+05 5.7 5.7 21 1.00E+07 4.96E+06 6.7 6.7 21 1.00E+08 4.96E+07 7.7 7.7 21 2.00E+08 9.92E+07 8   8.1 21

A graphical depiction of this result is shown in FIG. 16.

Summary Linearity:

The linear range, defined as the concentration range for which the log 10 deviation of the mean log 10 observed titers is within ±0.3 of the log 10 nominal titer was determined as: 4.87E+00 IU/mL-1.22E+08 IU/mL for EDTA-plasma and 3.90E+00 IU/mL-9.92E+07 IU/mL for serum.

5. Quantitative analysis of HIV

Mastermix

R1:

Final Conc. in 50 ul- Reagent PCR (uM) Mn(Ac)2 * 4H2O (pH 6.1 adjusted with Acetic Acid) 3′300 NaN3/Ri, buffered with 10 mM Tris at pH7 0.018 pH: 6.41

R2:

Final Conc. in Reagent 50 ul-PCR Glycerol (%, w/v)   3% Tricine  60 mM DMSO (%, v/v)  5.4% KOAc 120 mM Tween 20 (v/v) 0.02% Aptamer NTQ21-46 A 0.222 μM ZO5D Polymerase 0.9 U/μL (45 U/rxn) UNG 0.2 U/μL (10 U/rxn) Sodium Azide (w/v) 0.027    dCTPs   400 μM dGTPs   400 μM dATPs   400 μM dUTPs   800 μM Primers/probes selected from SEQ ID NOs 1-35 0.1 μM-0.3 μM SEQ ID NO 50  0.3 μM SEQ ID NO 51  0.3 μM SEQ ID NO 52 μM

Analytical Sensitivity/LOD

A dilution panel was prepared with HIV-1M Secondary Standard in HIV-1 negative EDTA plasma for sample input volumes of 200 μL and 500 μL. Each concentration level was tested with 21 replicates. At least >20 replicates have to be valid. The LOD was determined by PROBIT analysis at 95% hit rate and by >95% hit rate analysis.

TABLE 21 LOD analysis for 200 μL input volume in EDTA-plasma Number of Number of Concentration replicates positives Hit rate 200 cp/mL  21 21  100% 100 cp/mL  21 21  100% 80 cp/mL 21 21  100% 50 cp/mL 21 20 95.2% 30 cp/mL 21 18 85.7% 20 cp/mL 21 17 81.0% 10 cp/mL 21  8 38.1% 0 cp /mL (neg. control) 21  0   0% LOD by PROBIT analysis (95% hitrate) 41.8 cp/mL 95% confidence interval for LOD by 30.9-74.9 PROBIT analysis cp/mL

TABLE 22 LOD analysis for 500 μL input volume Number of Number of Concentration replicates positives Hit rate 30 cp/mL 21 21  100% 25 cp/mL 21 20 95.2% 20 cp/mL 21 21  100% 13.5 cp/mL   21 18 85.7%  9 cp/mL 21 13 61.9%  6 cp/mL 21  9 42.9% 0 cp /mL (neg. control) 21  0   0% LOD by PROBIT analysis (95% hitrate) 18.9 cp/mL 95% confidence interval for LOD by 14.9-29.4 PROBIT analysis cp/mL

Summary LOD

1. The PROBIT analysis at 95% hit rate resulted in an LOD of 41.8 cp/mL for 200 μL input volume and 18.9 cp/mL for 500 μL input volume.

2. The 95% confidence interval range for these concentrations was 30.9-74.9 cp/mL for 200 μL input volume and 14.9-29.4 cp/mL for 500 μL input volume.

Linearity

The samples used in the Linearity/Dynamic Range/Accuracy study consisted of a dilution panel of an HIV-1 cell culture supernatant material, HIV-1 group M subtype B.

The linearity panel was prepared by serial dilution. This panel was analyzed at 10 concentration levels.

The concentrations were selected as follows: One level below expected Lower Limit of Quantitation (LLoQ), one at LLoQ, one above LLoQ, several concentrations at intermediate levels, at expected Upper Limit of Quantitation (ULoQ) and one above ULoQ. For all concentrations 21 replicates were tested. The linearity study was done with 500 μL input volume):

PM 1—2.0E+07 cp/mL—above expected ULoQ

PM 2—1.0E+07 cp/mL—at expected ULoQ

PM 3—1.0E+06 cp/mL—below expected ULoQ

PM 4—1.0E+05 cp/mL—intermediate concentration level

PM 5 3.0E+04 cp/mL—intermediate concentration level for titer assignment

PM 6—1.0E+04 cp/mL—intermediate concentration level

PM 7—1.0E+03 cp/mL—intermediate concentration level

PM 8—1.0E+02 cp/mL—intermediate concentration level

PM 9—5.0E+01 cp/mL—above expected LLoQ

PM 10—2.0E+01 cp/mL—at expected LLoQ

PM 11—1.5E+01 cp/mL below expected LLoQ

TABLE 23 Linearity in EDTA Plasma Nominal Assigned Assigned Mean Log 10 Titer Titer Log10 Titer (cp/mL) (cp/mL) Titer observed Replicates 1.50E+01 1.50E+01 1.2 1.3 21 2.00E+01 2.00E+01 1.3 1.5 21 5.00E+01 5.10E+01 1.7 1.8 21 1.00E+02 1.00E+02 2 2 21 1.00E+03 1.00E+03 3 3 21 1.00E+04 1.00E+04 4 4 21 1.00E+05 1.00E+05 5 5 21 1.00E+06 1.00E+06 6 6 21 1.00E+07 1.00E+07 7 7 21 2.00E+07 2.00E+07 7.3 7.4 21

A graphical depiction of this result is shown in FIG. 17.

Summary Linearity

The linear range, defined as the concentration range for which the log 10 deviation of the mean log 10 observed titers is within ±0.3 of the log 10 nominal titer was determined as 1.5E+01 cp/mL-2.0E+07 cp/mL.

It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims. All publications, sequence accession numbers, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes. 

1-16. (canceled)
 17. A method for simultaneously isolating a plurality of different target nucleic acids from a plurality of different types of biological samples, wherein the plurality of different target nucleic acids is selected from a group consisting of bacteria, DNA viruses, and RNA viruses, the process comprising: (a) adding an identical lysis buffer to the biological samples in the vessels, wherein the number of vessels corresponds to the number of biological samples, wherein the lysis buffer comprises a chaotropic agent, a buffer substance, an alcohol, and a reducing agent, wherein the lysis buffer has a pH between 5.5 and 6.5; combining a solid support material with the biological samples for a period of time and under conditions sufficient to permit the target nucleic acids to be immobilized on the solid support material, wherein the period of time and conditions are identical for the plurality of biological samples; (b) isolating the solid support material of step (a) from other material that may be present in the biological samples; (c) washing the solid support material of step (b) with a wash buffer; and (d) separating the target nucleic acids from the solid support material; thereby simultaneously isolating the target nucleic acids from the plurality of biological samples.
 18. The method of claim 17, further comprising in step (d) adding an elution buffer.
 19. The method of claim 18, wherein step (d) is carried out at a temperature between 70° C. and 90° C.
 20. The method of claim 17, wherein the solid support material comprises nucleic acid binding particles.
 21. The method of claim 20, wherein the solid support material is magnetic glass particles.
 22. The method of claim 17, wherein step (a) is carried out at a temperature less than or equal to 50° C.
 23. The method of claim 17, further comprising: (e) transferring the target nucleic acids and optionally the solid support material to a plurality of reaction vessels; and (f) amplifying the target nucleic acids.
 24. The method of claim 17, further comprising in step (c), washing the solid support material one or more times with a wash buffer by aspirating and dispensing the suspension comprising wash buffer and the solid supporter material one or more times using a pipette.
 25. The method of claim 17, wherein the target nucleic acid is bacterial DNA.
 26. The method of claim 17, wherein the target nucleic acid is viral DNA.
 27. The method of claim 17, wherein the target nucleic acid is viral RNA.
 28. The method of claim 17, wherein the biological sample is a human body fluid.
 29. The method of claim 28, wherein the human body fluid is selected from a group consisting of: blood plasma, blood serum, whole blood, urine, sputum, sweat, swab, pipettable stool, and spinal fluid.
 30. The method of claim 29, wherein the human body fluid is blood plasma.
 31. The method of claim 29, wherein the human body fluid is blood serum.
 32. The method of claim 29, wherein the human body fluid is whole blood.
 33. The method of claim 29, wherein the human body fluid is urine.
 34. The method of claim 29, wherein the human body fluid is sputum.
 35. The method of claim 29, wherein the human body fluid is sweat.
 36. The method of claim 29, wherein the human body fluid is swab.
 37. The method of claim 29, wherein the human body fluid is pipettable stool.
 38. The method of claim 29, wherein the human body fluid is spinal fluid. 